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Glenmark Pharmaceuticals Ltd

Wed 21/05/2025,15:59:21 | NSE : GLENMARK

₹ 1440.103.90 (0.27%)

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Market Data

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Open

₹ 1428.10

Previous Close

₹ 1436.20

Volume

399837

Mkt Cap ( Rs. Cr)

₹40639.74

High

₹ 1464.10

Low

₹ 1427.10

52 Week High

₹ 1830.95

52 Week Low

₹ 1000.00

Book Value Per Share

₹ 299.28

Dividend Yield

0.17

Face Value

₹ 1.00

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77.57%

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13.34%

Sell

9.09%

77.57%

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News

Media spotlight triggers stock stock attention, sentiment.

  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Analyst / Investor Meet - Intimation

    19 May 2025, 10:29AM Enclosed please find herewith the details of Earnings Call slated for Monday, May 26, 2025 at 8:30 a.m. - 9:30 a.m. (IST), for your information and re
  • Glenmark Pharma - Analysts/Institutional Investor Meet/Con. Call Updates

    19 May 2025, 10:29AM Glenmark Pharmaceuticals Limited has informed the Exchange about Schedule of meet
  • Glenmark Pharma - Trading Window-XBRL

    12 May 2025, 4:35PM GLENMARK PHARMACEUTICALS LIMITED has informed the Exchange about Closure of Trading Window
  • Glenmark Pharma - Board Meeting Intimation

    12 May 2025, 4:31PM GLENMARK PHARMACEUTICALS LIMITED has informed the Exchange about Board Meeting to be held on 23-May-2025 to consider and approve the Yearly Audited Fi
  • Glenmark Pharma - Trading Window

    12 May 2025, 4:23PM Glenmark Pharmaceuticals Limited has informed the Exchange regarding the Trading Window closure pursuant to SEBI (Prohibition of Insider Trading) Regu
  • Glenmark Pharma - Board Meeting Intimation for Considering And Approving The Standalone And Consolidated Audited Financial Re

    12 May 2025, 4:19PM Glenmark Pharmaceuticals Ltdhas informed BSE that the meeting of the Board of Directors of the Company is scheduled on 23/05/2025 ,inter alia, to cons
  • Glenmark Pharma - General Updates

    9 May 2025, 10:34PM Glenmark Pharmaceuticals Limited has informed the Exchange about General Updates
  • Glenmark Pharma - Update On Glenmark'S Indore Manufacturing Facility

    9 May 2025, 10:31PM Kindly consider the attached update on Glenmark's Indore Manufacturing Facility.
  • Glenmark Pharma - Disclosure under SEBI Takeover Regulations

    7 May 2025, 12:09PM Glenmark Pharmaceuticals Limited has Submitted to the Exchange a copy of Disclosure under Regulation 31(4) of the Securities and Exchange Board of Ind
  • Glenmark Pharma - Press Release

    5 May 2025, 4:20PM Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated May 05, 2025, titled ""Ichnos Glenmark Innovation (IGI) Rec
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    5 May 2025, 4:21PM Ichnos Glenmark Innovation (IGI) receives U.S. FDA Fast Track Designation for ISB 2001 for Relapsed/ Refractory Multiple Myeloma
  • Glenmark Pharma - Rumour verification - Regulation 30(11)

    29 Apr 2025, 4:15PM Clarification/Confirmation on news item appearing in \Media/Publication\
  • Glenmark Pharma - News Verification

    29 Apr 2025, 4:10PM The Exchange has sought clarification from Glenmark Pharmaceuticals Limited with respect to recent news item captioned CDSCO Flags 70 Drug Batches, In
  • Glenmark Pharma - Format of the Annual Disclosure to be made by an entity identified as a LC - Annexure B2

    28 Apr 2025, 6:16PM <b>Format of the Annual Disclosure to be made by an entity identified as a Large Corporate.</b><br/><br/> <table border='1px'> <tr> <td><b>Sr
  • Glenmark Pharma - Clarification sought from Glenmark Pharmaceuticals Ltd

    28 Apr 2025, 6:00PM The Exchange has sought clarification from Glenmark Pharmaceuticals Ltd with reference to the media report appearing on https:// www.freepressjourna
  • Glenmark Pharma - News Verification

    28 Apr 2025, 5:54PM The Exchange has sought clarification from Glenmark Pharmaceuticals Limited with respect to recent news item captioned CDSCO Flags 70 Drug Batches, In
  • Glenmark Pharma - Format of the Initial Disclosure to be made by an entity identified as a Large Corporate : Annexure A

    28 Apr 2025, 5:54PM <b>Format of Initial Disclosure to be made by an entity identified as a Large Corporate.</b><br/><br/> <table border='1px'><tr> <td><b>Sr. No.</b></td
  • Glenmark Pharma - Shareholders meeting

    25 Apr 2025, 9:17PM Glenmark Pharmaceuticals Limited has submitted the Exchange a copy Srutinizers report of Postal Ballot. Further, the company has informed the Exchang
  • Glenmark Pharma - Shareholder Meeting / Postal Ballot-Outcome of Postal_Ballot

    25 Apr 2025, 9:15PM Voting result as required under Regulation 44(3) of SEBI Listing Regulations and Scrutinizers Report is enclosed.
  • Glenmark Pharma - Alteration Of Capital and Fund Raising-XBRL

    17 Apr 2025, 5:22PM Glenmark Pharmaceuticals Limited has informed the Exchange regarding Allotment of Securities
  • Glenmark Pharma - General Updates

    17 Apr 2025, 5:13PM Glenmark Pharmaceuticals Limited has informed the Exchange about Allotment of equity shares under the Glenmark Pharmaceuticals Limited Employee Stock
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Allotment of ESOP / ESPS

    17 Apr 2025, 5:05PM Allotment of Equity Shares under the Glenmark Pharmaceuticals Limited Employee Stock Option Scheme, 2016
  • Glenmark Pharma - Press Release

    16 Apr 2025, 7:30PM Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated April 16, 2025, titled ""Glenmark Pharmaceuticals Inc., USA
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    16 Apr 2025, 7:26PM Glenmark Pharmaceuticals Inc., USA to launch Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Ta
  • Glenmark Pharma has submitted to BSE the Shareholding Pattern for the Period Ended March 31, 2025

    16 Apr 2025, 5:42PM As of March 2025, 46.65% is owned by Indian Promoters and 53.35% by Public. <p align=justify> Institutional holds 37.75% (Insurance Companies 0.43%) a
  • Glenmark Pharma - Change in Directors/ Key Managerial Personnel/ Auditor/ Compliance Officer/ Share Transfer Agent

    7 Apr 2025, 12:03PM GLENMARK PHARMACEUTICALS LIMITED has informed the Exchange about Change in Directors/ Key Managerial Personnel/ Auditor/ Compliance Officer/ Share Tra
  • Glenmark Pharma - Cessation

    7 Apr 2025, 7:42AM Glenmark Pharmaceuticals Limited has informed the Exchange regarding Cessation of Mr. V.S. Mani as Executive Director of the company w.e.f. May 26, 2
  • Glenmark Pharma - Appointment

    7 Apr 2025, 7:42AM Glenmark Pharmaceuticals Limited has informed the Exchange regarding Appointment of Mr. Anurag Mantri as Senior Management of the company w.e.f. April
  • Glenmark appoints Anurag Mantri as President; V.S. Mani to step down as CFO

    7 Apr 2025, 10:36AM Glenmark Pharmaceuticals Ltd has announced the appointment of Mr. Anurag Mantri as President (Senior Management Personnel), effective April 7, 2025, f
  • Glenmark Pharma - Press Release

    1 Apr 2025, 8:55AM Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated April 01, 2025, titled ""Glenmark Pharmaceuticals Inc., USA
  • Glenmark Pharma launches Vancomycin Hydrochloride for injection in the U.S.

    1 Apr 2025, 12:02PM Glenmark Pharmaceuticals Inc., USA (Glenmark) has announced the launch of Vancomycin Hydrochloride for Injection USP in 750 mg/vial, 1.25 g/vial, and
  • Glenmark Pharma launches Vancomycin Hydrochloride for injection in the U.S.

    1 Apr 2025, 10:30AM Glenmark Pharmaceuticals Inc., USA (Glenmark) has announced the launch of Vancomycin Hydrochloride for Injection USP in 750 mg/vial, 1.25 g/vial, and
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    1 Apr 2025, 8:59AM Glenmark Pharmaceuticals Inc., USA launches Vancomycin Hydrochloride for Injection USP, 750 mg/vial, 1.25 g/vial and 1.5 g/vial (Single-Dose Vial)
  • Glenmark Pharma - General Updates

    28 Mar 2025, 11:47PM Glenmark Pharmaceuticals Limited has informed the Exchange about General Updates
  • Glenmark Pharma - Copy of Newspaper Publication

    27 Mar 2025, 4:31PM Glenmark Pharmaceuticals Limited has informed the Exchange about Copy of Newspaper Publication
  • Glenmark Pharma - Notice Of Shareholders Meetings-XBRL

    26 Mar 2025, 6:18PM GLENMARK PHARMACEUTICALS LIMITED has informed the Exchange about Notice of Shareholders Meeting for Postal Ballot
  • Glenmark Pharma - Shareholders meeting

    26 Mar 2025, 6:09PM Glenmark Pharmaceuticals Limited has informed the Exchange regarding Notice of Postal Ballot
  • Glenmark Pharma - Shareholder Meeting / Postal Ballot-Notice of Postal Ballot

    26 Mar 2025, 6:09PM Intimation regarding Postal Ballot Notice
  • Glenmark Pharma - Press Release

    20 Mar 2025, 8:53PM Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated March 20, 2025, titled ""Glenmark receives ANDA approval fo
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    20 Mar 2025, 8:41PM Glenmark receives ANDA approval for Olopatadine Hydrochloride Ophthalmic Solution USP, 0.2%
  • Glenmark Pharma - Press Release

    12 Mar 2025, 10:50AM Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated March 12, 2025, titled ""Glenmark Pharma Expands Cardiometa
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    12 Mar 2025, 10:50AM Glenmark Pharma Expands Cardiometabolic Portfolio with the Launch of Empagliflozin and its Fixed - Drug Combinations in India
  • Glenmark launches Empagliflozin-based diabetes medication &lsquo;Glempa&rsquo; in India

    12 Mar 2025, 12:10PM Glenmark Pharmaceuticals announced on Wednesday the launch of Empagliflozin, a widely recognized SGLT2 inhibitor, in India under the brand name Glempa
  • Glenmark Pharma - Press Release

    10 Mar 2025, 8:55AM Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated March 10, 2025, titled ""Glenmark Therapeutics Inc., USA la
  • Glenmark Introduces OTC Constipation Treatment in the US

    10 Mar 2025, 10:22AM Glenmark Pharmaceuticals announced on Monday the launch of its over-the-counter (OTC) constipation treatment, polyethylene glycol 3350, powder for sol
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    10 Mar 2025, 8:52AM Glenmark Therapeutics Inc., Polyethylene Glycol 3350
  • Glenmark Pharma - Press Release

    3 Mar 2025, 8:51AM Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated March 03, 2025, titled ""Glenmark Pharmaceuticals Inc., USA
  • Glenmark Expands U.S. injectable portfolio with acquisition and launch of Acetylcysteine injection

    3 Mar 2025, 9:03AM Glenmark Pharmaceuticals Inc., USA (Glenmark) has announced the acquisition and market launch of Acetylcysteine Injection, 6 gm/30 mL (200 mg/mL) Sing
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    3 Mar 2025, 8:49AM Glenmark Pharmaceuticals Inc., USA acquires and launches Acetylcysteine Injection, 6 gm/30mL (200mg/mL) Single-Dose Vials
  • Glenmark Pharma - Analysts/Institutional Investor Meet/Con. Call Updates

    27 Feb 2025, 4:30PM Glenmark Pharmaceuticals Limited has informed the Exchange about Schedule of meet
  • Glenmark Pharma - Press Release

    27 Feb 2025, 9:00AM Glenmark Pharmaceuticals Limited has informed the Exchange regarding a press release dated February 27, 2025, titled ""Glenmark Pharmaceuticals Inc.,
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Analyst / Investor Meet - Intimation

    27 Feb 2025, 4:31PM Details of Analyst/Institutional Investor Meeting is enclosed
  • Glenmark introduces Epinephrine injection in the US

    27 Feb 2025, 10:59AM Glenmark Pharmaceuticals announced on Thursday that it has introduced a generic version of the Epinephrine injection multiple-dose vial in the U.S., q
  • Glenmark Pharma - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    27 Feb 2025, 8:59AM Glenmark Pharmaceuticals Inc., USA launches Epinephrine Injection USP, 10 mg/ 10 mL (1 mg/mL) Multiple-Dose Vial
  • Glenmark Pharma - General Updates

    24 Feb 2025, 9:56AM Glenmark Pharmaceuticals Limited has informed the Exchange about General Updates
  • Glenmark Pharma - Disclosure Under Regulation 30 Of The SEBI (Listing Obligations And Disclosures Requirements) Regulations,

    24 Feb 2025, 9:58AM Disclosure under Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015: Glenmark Pharmaceuticals Ltd. (hereina
  • Glenmark Pharmaceuticals

    12 May 2025 , 11:25AM Glenmark Pharma: USFDA classified the Indore manufacturing unit after inspection as 'Official Action Indicated' (OAI).
  • Glenmark Pharma

    6 May 2025 , 8:58AM Ichnos Glenmark Innovation received USFDA fast-track status for ISB 2001, used to treat adult patients with relapsed or refractory multiple myeloma (a type of blood cancer).
  • Glenmark Pharmaceuticals

    17 Apr 2025 , 10:02AM The company plans to launch its Dextroamphetamine-Amphetamine tablets in USA, bioequivalent to Adderall, with distribution starting in May 2025. The tablets are used for attention deficit hyperactivity disorder (ADHD) treatment. Positive
  • Glenmark Pharma launches Acetylcysteine injection

    3 Mar 2025 , 10:27AM Glenmark Pharmaceuticals Inc., USA acquires and launches Acetylcysteine Injection, 6 gm/30 mL (200 mg/mL) Single-Dose Vials
  • Glenmark US arm launches Epinephrine injection multiple-dose vial

    27 Feb 2025 , 10:14AM Launch of Epinephrine injection multiple-dose vial is eligible for 180 days of CGT exclusivity
  • Glenmark Pharmaceuticals

    17 Feb 2025 , 8:57AM The USFDA conducted a GMP inspection at the company's manufacturing facility in Madhya Pradesh from Feb. 3, 2025 to Feb. 14, 2025, and issued a Form 483 with five observations. Negative
  • Glenmark pharma gets UK regulator's nod to market winlevi in the UK

    10 Feb 2025 , 12:00PM Cosmo, Glenmark announce UK MHRA approval of winlevi for treatment of Acne
  • Glenmark Pharmaceuticals US arm launches Phytonadione injectable emulsion USP.

    21 Jan 2025 , 9:48AM Phytonadione is used for blood clotting problems caused by Vitamin K deficiency.
  • Glenmark Pharmaceuticals Inc., USA launches Lacosamide Oral Solution

    16 Dec 2024 , 10:51AM Glenmark Pharma US unit launches Lacosamide oral solution used to treat seizures
  • Glenmark Therapeutics launches launches eye allergy drug in US

    19 Aug 2024 , 1:11PM Glenmark Therapeutics Inc., USA launches Olopatadine Hydrochloride Ophthalmic Solution USP
  • Glenmark Pharmaceuticals

    18 Jul 2024 , 1:05PM Glenmark Pharmaceuticals Ltd. (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Topiramate Capsules USP, 15 mg and 25 mg. Glenmark’s Topiramate Capsules USP, 15 mg and 25 mg has been determined by the FDA to be bioequivalent and therapeutically equivalent1 to Topamax®2 Capsules, 15 mg and 25 mg of Janssen Pharmaceuticals, Inc., and will be distributed in the U.S. by Glenmark Pharmaceuticals Inc., USA. (Positive)
  • Glenmark gets ANDA nod for Esomeprazole Magnesium Delayed-Release Capsules

    12 Jun 2024 , 10:24AM Esomeprazole Magnesium is used to treat certain stomach & Esophagus problems
  • Glenmark Pharma signs agreement with BeiGene for mktg & distribution

    21 May 2024 , 11:00AM Glenmark and BeiGene Enter into an Agreement for Marketing and Distribution of Tislelizumab and Zanubrutinib in India
  • Glenmark Pharma gets USFDA nod for brimonidine tartrate & timolol maleate ophthalmic solution

    17 May 2024 , 10:18AM Combigan Ophthalmic solution achieves annual sales of approximately $290.0 million
  • Glenmark receives ANDA approval for Acetaminophen and lbuproden Tablets

    29 Apr 2024 , 10:41AM Glenmark Pharma gets USFDA ANDA nod for Acetaminophen & Ibuprophen tablets
  • Glenmark Pharma

    31 Jan 2024 , 9:40AM Glenmark and Ichnos take a collaborative leap to accelerate innovation in Cancer Treatment with their alliance ‐ ‘Ichnos Glenmark Innovation’. This alliance brings together drug innovation capabilities of Glenmark and Ichnos to develop cutting‐edge therapies for the treatment of hematological malignancies and solid tumors. There are currently three oncology molecules in clinical trials, with two having received orphan drug designation from the U.S. FDA. The synergies derived from this alliance will substantially reduce Glenmark’s investment in innovative research. (Positive)
  • Glenmark Pharma inks license with Jiangsu Alphamab for KN035

    25 Jan 2024 , 10:26AM Glenmark signs licence agreement with Jiangsu Alphamab Bio, 3D med (Beijing) for KN035 for multiple geographies
  • Glenmark is the first to launch Biosimilar of Popular Anti-Diabetic Drug

    3 Jan 2024 , 10:12AM Glenmark Pharma launches anti-diabetic drug, Liraglutide in India under the brand name Lirafit
  • Glenmark Pharma launches a Triple-drug Fixed-Dose Combination

    18 Oct 2023 , 10:32AM Glenmark Pharma is first to launch a Triple-drug FDC of Teneligliptin + Dapagliflozin + Metformin in India
  • Glenmark Pharma enters into an agreement with Astria Therapeutics

    12 Oct 2023 , 9:47AM Glenmark Pharma enters into an agreement with Astria Therapeutics for antagonist monoclonal antibody portfolio
  • Glenmark signs distribution & license agreements with Cosmo Pharma

    27 Sep 2023 , 11:45AM Cosmo, Glenmark inks distribution and license agreements for Winlevi in abroad
  • Glenmark Pharma divests 75% stake in Glenmark Life

    22 Sep 2023 , 11:37AM Glenmark Pharma agrees to divest 75% stake in its subsidiary Glenmark Life Sciences to Nirma
  • Glenmark Pharmaceuticals

    22 Sep 2023 , 10:08AM The company has entered into a definitive agreement with Nirma Limited to divest 75% stake in its subsidiary, Glenmark Life Sciences (GLS) Limited at a price of Rs 615 (CMP – Rs 627) for an aggregate consideration of Rs 5,651.5 crs, subject to closing adjustments. Glenmark Pharma will continue to own 7.84% in GLS after the divestment. The transaction is subject to customary conditions precedent, including receipt of regulatory and shareholder approvals. Pursuant to the transaction, Nirma Limited will make a mandatory open offer to all public shareholders of GLS. The Acquirer announced the Open Offer to acquire the Equity Shares from the Public Shareholders of the Target Company, at a price of Rs. 631.20- per Equity Share aggregating to a total consideration of Rs. 1343 Crs payable in cash.
  • Glenmark Pharma gets US FDA nod for Tacrolimus Ointment

    17 Aug 2023 , 10:05AM Glenmark Pharma gets US FDA nod for Tacrolimus Ointment
  • Glenmark Pharmaceuticals

    22 Jun 2023 , 10:46AM The U.S. FDA has issued a warning letter to the Monroe facility in North Carolina. The company did a voluntary recall of all its products from this site in August 2021, and since then it has not been commercialising any products from this site. Hence, the warning letter will have no impact on the existing revenues, it said. Neutral read through.
  • Glenmark Pharma

    12 Apr 2023 , 10:44AM Glenmark Pharma is considering selling its majority stake of 82% in its unit Glenmark Life Sciences to curb its debt. Glenmark Lifesciences’ market value was Rs. 5,013 Cr or USD 611 million as of yesterday’s closing price valuing Glenmark’s stake at Rs. 4,110 Cr. while the company’s net debt stands at Rs. 2,615 Cr. as of Dec 22. It’s a positive development. We do not have coverage on it.
  • Glenmark Pharmaceuticals

    24 Mar 2023 , 11:59AM Glenmark Pharmaceuticals has received final approval from the US Food & Drug Administration (USFDA) for Calcipotriene and Betamethasone Dipropionate Foam, the generic version of Leo Pharma's Enstilar. It was an ANDA application with a paragraph IV certification, hence, with this approval, Glenmark is eligible for 180 days exclusivity. Positive development for the stock.
  • Glenmark Pharma gets final USFDA nod for Calcipotriene & Betamethasone Dipropionate foam.

    23 Mar 2023 , 9:42AM Calcipotriene & Betamethasone Dipropionate Foam is used to treat plaque psoriasis.
  • Glenmark receives US drug regulator nod for anti-sickness drug

    20 Mar 2023 , 10:24AM Glenmark Pharmaceuticals receives ANDA approval for Prochlorperazine Maleate Tablets USP, 5 mg and 10 mg
  • Glenmark Pharma

    17 Mar 2023 , 11:14AM Glenmark Pharma said its investigational new drug (IND) application for potential cancer drug was accepted by the USFDA. The USFDA approval enables Glenmark's subsidiary Glenmark Specialty to proceed with a Phase 1 and 2, first-in-human, clinical study of it. Positive development for the stock.
  • Glenmark Pharma

    17 Mar 2023 , 11:12AM Glenmark Pharma said its investigational new drug (IND) application for potential cancer drug was accepted by the USFDA. The USFDA approval enables Glenmark's subsidiary Glenmark Specialty to proceed with a Phase 1 and 2, first-in-human, clinical study of it. Positive development for the stock.
  • Glenmark Pharmaceuticals

    15 Mar 2023 , 10:27AM Glenmark Pharma has received approval from the USFDA to market generic anti-biotic drug called Clindamycin Hydrochloride Capsules in 75, 150 and 300 mg strengths, which will be distributed by Glenmark Pharma Inc. The drug had annual sales of USD 33.6 million as of Jan 23 as per IQVIA. Positive read through for the stock. We do not have it in the coverage.
  • Glenmark Pharma gets ANDA nod for Clindamycin Hydrochloride Capsules

    14 Mar 2023 , 12:02PM Clindamycin Hydrochloride capsules which are used to treat certain types of bacterial infections
  • Glenmark Pharmaceuticals

    9 Mar 2023 , 11:18AM Glenmark Pharmaceuticals said it has entered into an exclusive agreement with Cediprof Inc. for supply and distribution in the US for the latter's generic drug indicated for the treatment of attention deficit hyperactivity disorder. The agreement entered between Glenmark Pharmaceuticals Inc. USA and Cediprof Inc, a part of the Neolpharma Pharmaceutical Group family of companies, covers supply and distribution agreement for Cediprof's FDA-approved Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate tablets of strengths 5 mg, 10 mg, 15 mg, 20 mg and 30 mg, the company said in a statement. Positive read through for the stock. We do not have coverage on it.
  • Glenmark, Cediprof announce exclusive distribution agreement in US

    9 Mar 2023 , 10:30AM Glenmark expects to commence distribution of the product in the US during the second half of 2023
  • Glenmark Pharma gets tentative ANDA nod for Saxagliptin Tablets

    17 Feb 2023 , 9:54AM Glenmark Pharmaceuticals receives 2nd ANDA tentative approval for Saxagliptin Tablets, 2.5 mg and 5 mg
  • Glenmark Pharma launches Akynzeo IV in India

    23 Jan 2023 , 9:49AM Akynzeo IV is used to prevent chemotherapy-induced nausea & vomiting
  • Glenmark Pharma launches Sacubitril + Valsartan tablets in India

    17 Jan 2023 , 3:17PM Sacubitril + Valsartan tablets are used to treat heart failure
  • Glenmark Pharma launches Bumetanide Injection USP single & multi-dose vials in US

    10 Jan 2023 , 9:59AM Bumetanide Injection is used to treat fluid retention & swelling
  • Glenmark Pharma launches new type-II Diabetes Drug

    21 Dec 2022 , 10:22AM Glenmark is the first company to launch in India a Triple FDC of Teneligliptin + Pioglitazone + Metformin for Adults with Type 2 Diabetes & High Insulin Resistance
  • Glenmark Pharma gets ANDA nod for Nicardipine Hydrochloride Capsules

    19 Dec 2022 , 10:48AM Glenmark gets USFDA nod for Nicardipine Hydrochloride capsules used to treat high blood pressure
  • Glenmark Pharma

    24 Nov 2022 , 9:37AM The company stated that the USFDA has now issued a warning letter to the Goa (India) facility. It does not believe that the warning letter will have an impact on disruption of supplies or the existing revenues from operations of this facility.The Company is committed to work along with the US FDA to implement all the necessary corrective actions required to address the concerns at the earliest. The Company is committed to maintaining the highest quality and compliant manufacturing standards at all of its facilities across the globe.
  • Glenmark settles agreement with Pfizer for Axitinib Tablets

    22 Nov 2022 , 9:50AM Glenmark Pharmaceuticals reaches settlement agreement with Pfizer for Axitinib Tablets, 1 mg and 5 mg
  • Glenmark Pharma launches Teneligliptin + Dapagliflozin Fixed Dose Combination for Type-2 diabetes

    20 Oct 2022 , 10:52AM With this new launch, the company aims to improve glycemic control in adult patients
  • Glenmark Pharmaceuticals

    20 Oct 2022 , 10:17AM Glenmark Pharmaceuticals is the first company in India to launch Teneligliptin (20mg) + Dapagliflozin (5mg/10mg) fixed dose combination (FDC) for the treatment of adult patients with type 2 diabetes, especially the ones with comorbidities. Marketed under the brand name Zita D; it contains Teneligliptin (20mg) + Dapagliflozin (5 mg/10 mg) and must be taken once daily under prescription to improve glycemic control & prevent complications in adult patients with type 2 diabetes, especially the ones with comorbidities. Positive read-thru.
  • Glenmark Pharma launches Lobeglitazone in India for uncontrolled type-2 diabetes in adults

    6 Oct 2022 , 11:24AM Glenmark becomes the First Pharmaceutical Company to launch Lobeglitazone in India for Uncontrolled Type 2 Diabetes in Adults
  • Glenmark Pharma

    23 Sep 2022 , 10:35AM Following the inspection in June 2022, the US FDA had issued a Form-483 with six observations to Baddi facility. The company believes it is unlikely to have any material impact on the US business at this stage. The Company is committed to maintaining the highest quality and compliant manufacturing standards at all of its facilities across the globe. On the other hand its Aurangabad facility has received (EIR) Establishment Inspection Report from the USFDA indicating closure of the inspection.
  • Bausch Health, Glenmark announce approval of RYALTRIS in Canada

    23 Sep 2022 , 9:47AM Glenmark Pharma says Health Canada approves Ryaltris for treatment of seasonal allergic rhinitis
  • Glenmark Pharma

    23 Sep 2022 , 9:40AM Bausch Health and Glenmark have announced the approval of RYALTRIS® in Canada. RYALTRIS® (olopatadine hydrochloride and mometasone furoate nasal spray) treats moderate to severe seasonal allergic rhinitis (SAR) and associated ocular symptoms in adults, adolescents, and children aged 6 years and older. RYALTRIS is a fixed-dose combination therapy that provides relief for the symptoms of SAR, both nasal and ocular, in one easy-to-use nasal spray. The onset of action for nasal symptom relief occurs within 15 minutes after administration of RYALTRIS. Positive for the stock.
  • Glenmark Pharmaceuticals

    29 Aug 2022 , 10:11AM The USFDA has inspected the company’s Goa plant in between 12 May 2022 to 20 May 2022 and has issued a form 483 with five observations then. Now the USFDA has communicated to Glenmark that it has classified this above said inspection as OAI (Official Action Indicated), which implies that the USFDA may withhold approval of any pending product applications or supplements filed from this facility till the outstanding observations are resolved. Negative read thru, though we do not have a coverage on the stock
  • Glenmark Pharmaceuticals

    24 Aug 2022 , 10:02AM The USFDA has inspected the company’s North Carolina facility in the US from April 04 to May 19, 2022 and the inspection ended with a issuance of form 483 and 17 observations. Recently the USFDA has classified this inspection as OAI (Official Action Inidcated), which implies that the USFDA may with hold product applications / supplements filed from this site. Negative though we do not have a coverage on the stock
  • Strides Pharma, Cipla , Glenmark

    22 Aug 2022 , 11:20AM Strides Pharma, Cipla and Glenmark: are recalling products from US markets. Strides Pharma is recalling 1,032 bottles of Prednisone tablets, a medication used to treat many conditions including asthma, allergic reactions, arthritis, inflammatory bowel diseases. As per the USFDA, the company is recalling the affected lot due to "presence of foreign tablet. Cipla is recalling 7,992 bottles of Difluprednate Ophthalmic Emulsion, used to treat swelling and pain after eye surgery, in the US market. As per USFDA the reason for recall by Cipla is lack of assurance of sterility and also for Defective Container Closure. Glenmark is recalling over 72,000 units of blood pressure lowering drug due to reasons of "blister package issues". All of the three recalls have been classified as class II recalls and hence it is not likely to have any material impact on the financials of the companies
  • Glenmark Pharma gets USFDA nod for Norethindrone Acetate & Ethinyl Estradiol Capsules

    29 Jul 2022 , 9:54AM Glenmark Pharma gets USFDA nod for a birth control pill, Norethindrone Acetate & Ethinyl Estradiol Capsules
  • Glenmark Pharmaceuticals launches MINYM GEL

    11 Jul 2022 , 10:20AM Glenmark Pharma launches topical Minocycline Gel for treatment acne
  • Glenmark Pharma launches Sitagliptin & its fixed dose combinations

    7 Jul 2022 , 12:48PM Glenmark launches Sitagliptin and its Fixed Dose Combinations, at affordable price for adults with type 2 Diabetes in India
  • Glenmark Pharmaceuticals

    4 Jul 2022 , 9:43AM The company’s Aurangabad facility was inspected by the USFDA between June 27, 2022 and July 1, 2022 and the inspection ended with a Form 483 being issued with one observation. Though the management is committed to undertake the required steps to resolve the observation, but receipt of form 483 is negative.
  • Glenmark Pharma acquires ANDAs from Wockhardt

    28 Jun 2022 , 10:25AM Glenmark Pharma acquires ANDAs for Famotidine Tablets from Wockhardt in US
  • Glenmark Pharmaceuticals

    23 Jun 2022 , 10:43AM Glenmark: The company’s Baddi manufacturing facility which is a formulations manufacturing facility was inspected by the USFDA between 13 June 2022 and 22 June 2022 and the inspection ended with a Form 483 and 6 observations being issued. While the company is committed to resolve the observations issued at the earliest, but the receipt of Form 483 with 6 observations is a negative read thru.
  • Glenmark to launch Indacaterol + Mometasone fixed-dose combination drug for Asthma in India

    16 Jun 2022 , 10:18AM Glenmark becomes the First Pharmaceutical Company to launch Indacaterol + Mometasone Fixed-Dose Combination Drug for Asthma in India
  • Glenmark Pharmaceuticals

    23 May 2022 , 11:01AM The company’s Monroe facility at the US was inspected by the USFDA between 4 April 2022 to 19 May 2022. The inspection ended with form 483 and 17 Observations. Also the USFDA inspected the company’s Goa plant between 12 May2022 to 20 May 2022. The inspection ended with the Form 483 being issues with five observations. The receipt of Form 483 with observations is negative for Glenmark. We do not have a coverage on the stock.
  • Glenmark Pharma gets sANDA nod for Abiraterone Acetate Tablets USP, 500 mg

    20 May 2022 , 9:38AM Glenmark Pharma received USFDA approval for Abiraterone Acetate Tablets, used to treat prostate cancer
  • Glenmark Pharma gets tentative ANDA nod for Calcipotriene and Betamethasone Dipropionate Foam

    9 May 2022 , 9:44AM Calcipotriene & Betamethasone Dipropionate Foam, used for topical treatment of plaque psoriasis in adults
  • Glenmark to launch Teneligliptin + Pioglitazone fixed‐dose drug for type-2 Diabetes in India

    25 Apr 2022 , 9:58AM Launches under the brand name Zita Plus Pio, will increase the accessibility of quality drug for effective diabetes management
  • Glenmark Pharmaceuticals

    5 Apr 2022 , 11:17AM Glenmark: The company’s Operations Committee at its meeting approved to repurchase bonds by way of on market purchases at an early redemption amount, aggregating to principal amount of $75 mn (~Rs 560 cr) issued in 2016, along with accrued and unpaid interest. The repurchase of the bonds would enables to reduce the company’s high debt levels and so its positive, though we don’t have any coverage on the stock.
  • Glenmark Pharma gains momentum

    23 Mar 2022 , 12:39PM Glenmark Pharma rises over 2% to Rs. 461, in trade
  • Glenmark inks agreement with Astrazeneca

    14 Feb 2022 , 2:08PM Glenmark inks agreement with Astrazeneca to commercialise its product Pulmicort Respules in Colombia
  • Glenmark Pharma launches nasal spray for treatment of Covid patients in India

    9 Feb 2022 , 10:39AM Glenmark receives manufacturing and marketing approval from India’s drug regulator for Nitric Oxide Nasal Spray
  • Glenmark Pharma arm enters into licensing agreement with Lotus Intl

    20 Jan 2022 , 10:22AM Glenmark Pharma arm enters into licensing agreement with Lotus Intl for Ryaltris Nasal Spray in Singapore, Hong Kong, and Vietnam
  • Glenmark Pharmaceuticals

    17 Jan 2022 , 10:44AM Glenmark: US arm of the company - Glenmark Pharmaceuticals Inc., USA, has received tentative approval from the USFDA for Regadenoson Injection, 0.4 mg/5 mL (0.08 mg/mL) Single-Dose Pre-Filled Syringe, which is a generic version of Lexiscan injection. As per IOVIA sales data for the 12 month period ending November 2021 for Lexiscan injection stood at $659.9 mn, which is substantial, hence the tentative approval is positive
  • Glenmark gets USFDA nod for Ryaltris nasal spray

    14 Jan 2022 , 9:45AM Glenmark's Swiss arm gets USFDA nod for Ryaltris nasal spray, used to treat allergic rhinitis in adults
  • Glenmark Pharmaceuticals

    24 Dec 2021 , 1:13PM CRISIL ratings has upgraded the long term ratings for Glenmark from “CRISIL AA-/Stable” to “CRISIL AA-/Positive” while it has reaffirmed the short term ratings of “CRISIL A1+”. Positive read thru as the outlook on the long term ratings has been upgraded to positive.
  • Glenmark Pharmaceuticals

    15 Nov 2021 , 3:19PM Reports in line set of results for Q2FY22 with the sales 3147.4 cr up by 6.6% and the revenues were in line with the estimates. The company reported healthy growth across key markets in Central Europe. The gross margins declined by 110 bps yoy while savings in employee cost led the OPM to be flat at 18.8%. the adjusted PAT at Rs 274 cr up by 17.5% and is in line with the street’s estimates.
  • Glenmark launches dry powder inhaler Tavulus in Spain

    11 Oct 2021 , 10:03AM Tiotropium Bromide dry powder inhaler (DPI) is used to treat chronic obstructive pulmonary disease
  • Aurobindo, Glenmark

    4 Oct 2021 , 11:00AM In the US markets, Glenmark is recalling 28,658 cartons of Fulvestrant injection (a breast cancer medicine) and 11,000 units of Arformoterol Tartrate Inhalation Solution due to "lack of assurance of sterility. It is also recalling 9,552 bottles of 275 MG strength and 31500 bottles of 550 Mg strength of Naproxen Sodium Tablets (pain reliving tablet) and 6,552 bottles of Chlorzoxazone tablets (for muscle relaxations) due to GMP deviations. Aurobindo’s US arm - Aurobindo Pharma USA Inc is recalling 2,820 bottles of Metoprolol tartrate tablets (used to treat high blood pressure)due to presence of foreign substance. Recalls by both the company’s are classified as Class II recalls and hence unlikely to have any material impact on their financial performance.
  • Glenmark receives marketing approval for Ryaltris

    30 Sep 2021 , 9:49AM Ryaltris is a fixed dose combination nasal spray that combines an antihistamine (Olopatadine) with a steroid (Mometasone Furoate) for treatment of allergic rhinitis
  • Glenmark Pharmaceuticals

    16 Aug 2021 , 9:34AM Glenmark - Q1FY22 Results: Glenmark reported a strong set of results and the PAT coming ahead of street estimates. The consolidated revenues at Rs 2964 cr were up by 26.4% YoY driven by a 57% yoy growth in the India business driven by a covid led products like Favipiravir. Operating margins at 19.3% were higher than the estimates 18.6% but declined by 100 bps yoy due to gross margins contraction. The operating profits at Rs 573 cr grew 20% yoy and was slightly ahead of street estimates of Rs 554 cr. The Adjusted PAT at Rs 306.5 cr was up 35.6% yoy driven by a 19% decline interest cost and was ahead of street estimates of Rs 261 cr.
  • Glenmark Pharmaceuticals

    22 Jul 2021 , 9:34AM Glenmark Lifesciences is coming out with an IPO through a fresh issue of Rs 1060 cr and offer for sale by Glenmark of 63 lakh shares. The price band is fixed at Rs 695-720 per share and the Glenmark Life Sciences plans to raise Rs 1513.6 crore through the IPO. This provides an value unlocking opportunity for Glenmark shareholders and hence positive.
  • Glenmark Pharmaceuticals

    7 Jul 2021 , 10:57AM Glenmark: Has joined hands with with the Canadian company- Sanotize for its Nitric Oxide nasal spray which it claims is effective against Covid and so the company had sought emergency approval from the drug regulator for the import and marketing of nasal spray in to India. The Drug regulator has asked Glenmark to conduct Phase III trial on nitric oxide nasal spray. If the trials are successful and the products gets approval, it would be positive as the product would further strengthen the company’s Covid portfolio.
  • Glenmark gets tentative USFDA approval for cancer drug, Nintedanib Capsule

    25 Jun 2021 , 9:47AM Glenmark Pharmaceuticals receives ANDA tentative approval for Nintedanib Capsules, 100 mg and 150 mg
  • Glenmark Pharmaceuticals

    23 Jun 2021 , 10:45AM Glenmark: Received USFDA approval for Arformoterol Tartrate Inhalation Solution (Unit-Dose Vials), the generic version of BROVANA Inhalation Solution. The product would be manufactured by the company at its North American facility. As per IQVIA, for the 12 month period ending April 2021 Brovana inhalation solution achieved annual sales of $ 437.9 mn. Given the strong addressable market size, the approval is positive.
  • Glenmark Pharma gets USFDA nod for Arformoterol Tartrate Inhalation Solution

    23 Jun 2021 , 10:37AM It will be manufactured in the company’s North American manufacturing facility based in Monroe, North Carolina
  • Glenmark launches Tiogiva

    15 Jun 2021 , 2:44PM Drug is bioequivalent version of Tiotropium Bromide dry powder inhaler
  • Glenmark Pharmaceuticals

    9 Jun 2021 , 10:32AM Glenmark: Has announced an interim data from its Post Marketing Surveillance study on Favipiravir in India. The study is the first and large post marketing study being conducted in India on Favipiravir in mild to moderate Covid-19 patients and the interim data supports the safety and effectiveness of FabiFlu in real-world settings and indicates no new safety concerns. The fact that there are no new safety concerns observed with Fabiflu in a Post marketing Surveillance study is positive
  • Glenmark Pharmaceuticals

    31 May 2021 , 11:27AM Glenmark: reported inline results for Q4FY2021. The revenues at Rs 2859.8 cr grew by 3.3% YoY backed by a 7.7% and a 5.2% yoy growth at the India as well as the US business. The operating margins stood at 18.3% which is an expansion of 150 bps yoy led by a 250 bps gross margins expansion. The operating profit at Rs 523.5 cr grew by 12.4% yoy. The other income for the quarter declined by 80.8% yoy to Rs 8.5 cr, while the interest and the depreciation charges also declined by 15% and 12% yoy respectively. Consequently, the adjusted PAT stood at RS 233.9 cr up by 24.8% yoy and was largely in line with the estimates. The company has filed for 7 ANDA’s in the FY2021 and due to Covid pandemic few of its fillings have been pushed ahead in FY22. Further the company has guided for 18-20 fillings in FY22.
  • Glenmark Pharmaceuticals receives ANDA nod for Icatibant Injection

    24 May 2021 , 9:42AM Glenmark Pharma gets approval from USFDA for Icatibant Injection, Single-Dose Prefilled Syringe, the generic version of Firazyr Injection
  • Glenmark launches Ryaltris-AZ at an affordable price in India

    3 May 2021 , 10:44AM Glenmark Pharma launches Ryaltris-AZ Nasal Spray for the treatment of moderate to severe allergic rhinitis, in India
  • Glenmark Pharmaceuticals

    3 May 2021 , 10:21AM Glenmark: The company has invested Rs 40 cr to acquire a 6.45% stake in ABCD Technologies LLP, which is a recently incorporated entity and yet to commence activity. Initiative with an objective to facilitate, enable and promote efficiency and Good Distribution Practices including digitizing healthcare infrastructure in India, inter alia, in support of the National Digital Health Mission
  • Glenmark Pharmaceuticals

    26 Apr 2021 , 2:17PM Glenmark: Gets approval from the European Union for its innovative nasal spray - Ryaltris (olopatadine hydrochloride 665 mcg and mometasone furoate 25 mcg). The approval would enable the company to launch the spray in 17 EU countries. In few of the markets Glenmark would commercialize Ryaltris while in rest of the markets Menarini Group will commercialize. As per the terms of agreement, Glenmark is responsible for the continued development and regulatory approval of Ryaltris in these markets, while Menarini will lead the scientific information and commercialization of Ryaltris, following regulatory approval. The approval is positive as it opens up a new market for Ryaltris and would also add to the overall topline of the company
  • Glenmarks Ryaltris nasal spray approved in Europe

    26 Apr 2021 , 2:01PM Glenmark’s Ryaltris nasal spray is approved in Europe for the first line treatment of allergic rhinitis in patients over 12 years of age
  • Glenmark Pharmaceuticals

    19 Apr 2021 , 11:18AM Wholly owned subsidiary of the company – Glenmark Life Sciences Limited, has filed a draft red herring prospectus with the SEBI for an IPO comprising a fresh issue of Rs 1160 cr and an offer for sale of 73,05,245 equity share of FV Rs 2 by Glenmark Pharmaceuticals Limited. The IPO is subject to receipt of the applicable approvals and could help Glenmark reduce its debt.
  • Glenmark Pharmaceuticals

    24 Mar 2021 , 1:49PM Gets USFDA approval for Chlorpromazine Hydrochloride Tablets USP strength - 10 mg, 25 mg, 50 mg, 100 mg, and 200 mg. The tablets are generic version of Thorazine tablets. The USFDA has granted competitive generic therapy (CGT) designation for the drug which means that Glenmark is the first approved applicant for such competitive generic therapy and is eligible for 180 days of CGT exclusivity upon commercial marketing. As per IQVIA sales data for 12 month ending Jan 2021, Thorazine tablets achieved annual sales of approximately $108.6 mn. Given the CGT status for the approval and the healthy market potential, the approval is positive
  • Glenmark Pharmaceuticals

    24 Mar 2021 , 12:16PM Gets USFDA approval for Chlorpromazine Hydrochloride Tablets USP strength - 10 mg, 25 mg, 50 mg, 100 mg, and 200 mg. The tablets are generic version of Thorazine tablets. The USFDA has granted competitive generic therapy (CGT) designation for the drug which means that Glenmark is the first approved applicant for such competitive generic therapy and is eligible for 180 days of CGT exclusivity upon commercial marketing. As per IQVIA sales data for 12 month ending Jan 2021, Thorazine tablets achieved annual sales of approximately $108.6 mn. Given the CGT status for the approval and the healthy market potential, the approval is positive
  • Glenmark gets USFDA nod for a schizophrenia drug

    24 Mar 2021 , 9:41AM Glenmark gets USFDA nod for Chlorpromazine Hydrochloride tablets, used to treat Schizophrenia
  • Glenmark Pharmaceutical

    22 Mar 2021 , 12:55PM Glenmark: Subsidiary company - Glenmark Specialt SA - Switzerland and an affiliate of Bausch Health Companies Inc. have entered into an exclusive licensing agreement for the commercialization of Glenmarks nasal spray - RYALTRIS in Canada. The product is proposed indication for seasonal allergic rhinitis and is under review by regulator – Health Canada. As per the terms of the agreement, Glenmark would be responsible for the regulatory approval and Bausch Health Canada would be responsible for the commercialization of the product following regulatory approval. Also Glenmark would be entitled for an upfront payment, launch & sales‐based milestone payments in addition to royalties and supply price from sales of RYALTRIS. The agreement is positive as it opens up a new market for Ryaltris and would also add to the overall topline of the company.
  • Glenmark, Bausch Health partner to commercialise RYALTRIS nasal spray in Canada

    22 Mar 2021 , 10:56AM Glenmark will receive an upfront payment, launch & sales‐based milestone payments in addition to royalties and supply price from sales of RYALTRIS
  • Glenmark Pharmaceuticals

    19 Mar 2021 , 10:25AM The company shall be issuing an invitation to the holders of its outstanding USD 200 mn, 2% bonds due 2022 for purchase by the company for cash consideration. The bonds were issued in 2016.
  • Glenmark Pharmaceuticals

    22 Feb 2021 , 9:37AM Glenmark: Swiss subsidiary -Glenmark Specialty S.A., gets marketing approval from the Ministry of Health of the Russian Federation for its innovative Ryaltris Nasal Spray , which is a novel fixed-dose combination nasal spray. The authorization paves the way for commercialization of Ryaltris in Russia, which the company expects to be made available to patients in Q1FY2022. Ryaltris relieves patients from the symptoms of allergic rhinitis, including stuffy nose, runny nose, nasal itching, sneezing, as well as itchy, red and watery eyes. The approval is positive as Ryaltris launch would strengthen the Russian revenues
  • Glenmark Pharma launches SUTIB

    16 Feb 2021 , 10:08AM Glenmark Pharma launches SUTIB, the generic version of Sunitinib oral capsules to treat kidney cancer in India
  • Glenmark Pharmaceuticals receives ANDA nod for Clindamycin Phosphate Gel USP

    11 Feb 2021 , 10:35AM Glenmark Pharma gets USFDA nod for Clindamycin Phosphate Gel, used for topical application in the treatment of acne vulgaris
  • Glenmark Pharma gets ANDA nod for Topiramate Extended-Release Capsules

    3 Feb 2021 , 10:45AM Glenmark Pharmaceuticals receives ANDA approval for Topiramate Extended-Release Capsules
  • Glenmark Pharma gets ANDA nod for Amphetamine Sulfate tablets

    28 Jan 2021 , 9:40AM Glenmark Pharma gets USFDA nod for Amphetamine Sulfate tablets used for treatment of attention deficit hyperactivity disorder
  • Glenmark Pharmaceuticals

    5 Jan 2021 , 11:01AM Glenmark Pharmaceuticals : Has issued a notice of optional redemption to the holders of U.S. $200 million 4.5% Senior Notes due 2021 listed on the Singapore Exchange Securities Trading Limited. The company has elected to redeem $10,000,000 aggregate principal amount outstanding of its 4.5% Senior Notes due 2021. The record date for redemption is 14th January 2021.
  • Glenmark Pharmaceuticals

    5 Jan 2021 , 11:00AM Glenmark Pharmaceuticals : Has issued a notice of optional redemption to the holders of U.S. $200 million 4.5% Senior Notes due 2021 listed on the Singapore Exchange Securities Trading Limited. The company has elected to redeem $10,000,000 aggregate principal amount outstanding of its 4.5% Senior Notes due 2021. The record date for redemption is 14th January 2021.
  • Glenmark gets USFDA nod for Tadalafil Tablets

    31 Dec 2020 , 11:23AM It has also obtained tentative approval for Gabapentin Enacarbil Extended Release Tablets
  • Glenmark Pharmaceuticals and Menarini enter into Exclusive Licensing Agreement

    23 Dec 2020 , 11:13AM The licensing agreement will be effective in 33 countries throughout the European region including France, Italy, and Spain
  • Glenmark receives USFDA approval for Dabigatran Etexilate Capsules

    21 Dec 2020 , 9:49AM Glenmark Pharmaceuticals receives ANDA tentative approval for Dabigatran Etexilate Capsules, 75 mg, 110 mg, and 150 mg
  • Glenmark Pharmaceuticals

    14 Dec 2020 , 2:09PM The company has redeemed 4.5% Senior Notes due 2021, amounting $ 7500,000. Earlier the company had redeemed $182.5 mn worth of notes. Post the recent redemption, notes amounting to $10 mn are outstanding of the total $200 mn worth of notes. .
  • Glenmark Pharmaceuticals

    10 Dec 2020 , 12:48PM Glenmark: Has redeemed its 4.5% senior noted to the tune of $182.5 mn in aggregate principal amount representing 91.25% of the aggregate 2021 principal notes due for redemption.
  • Glenmark Pharma gets USFDA tentative approval

    1 Dec 2020 , 10:32AM Glenmark Pharmaceuticals receives ANDA tentative approval for Axitinib Tablets, 1 mg and 5 mg
  • Dr Reddy’s, Glenmark

    1 Dec 2020 , 10:10AM Dr Reddy’s to acquire brands in the anti allergy space for Russian and CIS countries; acquisition is positive as it would strengthen Dr Reddys presence in the anti allergy space in these countries.
  • Glenmark gets position in Dow Jones

    26 Nov 2020 , 2:55PM Glenmark Pharmaceuticals secures its position in the prestigious Dow Jones Sustainability Emerging Markets Index for the third year in a row
  • Glenmark Pharmaceuticals

    25 Nov 2020 , 10:27AM S&P global ratings have affirmed its long-term issuer credit rating on Glenmark and the issue rating on the company's US$200 million senior unsecured notes at 'BB-'. Also the agency has removed all the ratings from “CreditWatch” category due to subsiding of refinancing risks as the company has raised US$182.5 mn in November 2020 via a term loan to redeem a similar amount of its $200 million senior unsecured notes due Aug. 2, 2021. Removal from Credit Watch category is positive
  • Glenmark Pharmaceuticals

    11 Nov 2020 , 11:55AM Glenmark: The company has received an approval from the USFDA for Tacrolimus Capsules USP, 0.5 mg, 1 mg and 5 mg. Tacrolimus Capsules are the generic versions of Prograf Capsules, which has reported an annual sales of approx $286.8 mn as of the 12 month period ending September 2020 according to IQVIA. The approval is positive as it would help improve the US revenues.
  • Glenmark Pharma gets ANDA approval

    11 Nov 2020 , 10:19AM Glenmark Pharmaceuticals receives ANDA approval for Tacrolimus Capsules USP, 0.5 mg, 1 mg and 5 mg
  • Glenmark gets USFDA nod for an immunosuppressant

    19 Oct 2020 , 10:32AM Glenmark Pharmaceuticals receives ANDA approval for Sirolimus Tablets, 0.5 mg, 1 mg and 2 mg
  • Glenmark Pharmaceuticals

    14 Oct 2020 , 10:40AM Glenmark: launched NINDANIB (Nintedanib 100 mg and 150 mg capsules) for the treatment of pulmonary fibrosis in India. Glenmark is a leader in the area of respiratory has been amongst the first to launch the branded generic version at an affordable cost for the treatment of Pulmonary Fibrosis in India. Glenmark’s NINDANIB priced at Rs. 4500 (100 mg) and Rs. 5400 (150 mg) PER MONTH is just available at 5 % of the cost as compared to the innovator brand in India. The disease affects around 120 Indians per million. The product launch could add to the revenues of the India business
  • Glenmark introduces Nintedanib for treatment of Pulmonary Fibrosis

    14 Oct 2020 , 10:05AM Glenmark Pharmaceuticals launches Nintedanib 100 and 150 mg capsules for the treatment of pulmonary fibrosis in India
  • Glenmark gets ANDA nod for Dimethyl Fumarate Delayed-Release Capsules

    7 Oct 2020 , 10:12AM Glenmark Pharma gets USFDA nod for Dimethyl Fumarate Delayed-Release Capsules, used for treatment of Multiple Sclerosis
  • Glenmark Pharmaceuticals

    7 Oct 2020 , 9:39AM Gets USFDA approval for Dimethyl Fumarate Delayed-Release Capsules – 120 mg and 240 mg for the US market. The medicine is indicated for the treatment of multiple sclerosis. The reference listed drug - Tecfidera had annual sales of approx. $3.8 bn in the US for the 12 months ending August 2020. The approval is positive as it would add to the US sales.
  • Glenmark Pharmaceuticals

    17 Aug 2020 , 10:09AM Glenmark Q1FY2021 Result: strong operational performance
  • Glenmark Pharmaceuticals

    6 Aug 2020 , 2:44PM To introduce a 400 mg version of oral antiviral tablet - FabiFlu, for the treatment of mild to moderate COVID-19 patients in India. Earlier the company had launched a 200 mg version of the tablet. The higher strength tablet will improve patient compliance and experience, by effectively reducing the number of tablets that patients require per day. Given te increase in count of Covid patients, the demand for the tablet could rise
  • Glenmark Pharmaceuticals

    30 Jul 2020 , 9:54AM S&P global ratings have placed Glenmark’s long term issuer credit ratings and that on company’s notes to “BB- under Credit watch with Negative implicatons” on growing refinance risk. The company has s several bullet debt maturities totaling US$340 million in 2021 (around Rs 2544 crore), including a put option on its foreign currency convertible bonds. Due substantial funding requirements and challenging market conditions could strain ability to raise funds, significantly weakening its liquidity.
  • Glenmark Pharmaceuticals

    23 Jul 2020 , 10:04AM Announced results from a Phase 3 clinical trial in mild to moderate COVID-19 patients conducted across seven clinical sites in India. The trial conducted in 150 patients, evaluated the efficacy and safety of Favipiravir plus standard supportive care (Favipiravir treatment arm), versus standard supportive care alone in mild to moderate Covid 19 patients. Results from the Phase 3 trial showed improvements for the primary efficacy endpoint with 28.6% faster viral clearance in the overall population as measured by the median time. Better results from the trial is positive.
  • Glenmark Pharmaceuticals

    20 Jul 2020 , 10:05AM the DCGI (drug controller general of India) has issued notices to Glenmark seeking clarification regarding the false claim that its antiviral drug Fabiflu, is effective on COVID-19 patients with co-morbidities. Glenmark has claimed that this drug is effective in co-morbid conditions like hypertension, diabetes. As per protocol summary, this trial was not designed to assess Fabiflu in co-morbid conditions. No clinically sufficient data specific to these conditions are available. If the allegations are established, then it could adversely impact Glenmarks earnings and is negative for Glenmark
  • Glenmark

    13 Jul 2020 , 11:53AM Fitch has affirmed Glenmark Pharmaceuticals Long-Term Issuer Default Rating at 'BB'. The Outlook is Stable. Fitch has also affirmed Glenmark's USD 200 million 4.50% senior unsecured notes due 2021 at 'BB'. The notes are rated at the same level as the IDR because they constitute Glenmark's direct and senior unsecured obligations. The rating affirmation factors in company’s geographic diversification and satisfactory record of regulatory compliance, adequate product pipeline and robust long term growth prospects in India.
  • Glenmark announces price reduction of 27% for Fabiflu drug

    13 Jul 2020 , 11:22AM Glenmark announces price reduction of 27% for FabiFlu drug, new MRP at Rs. 75/tab Vs Rs. 103/tab earlier
  • Glenmark Pharmaceuticals

    1 Jul 2020 , 12:04PM As per media reports, there is a case against Glenmark in the US in the federal court of Philadelphia. The prosecutor has said that the company has conspired with competitors to raise the prices of generic drugs and that Glenmark colluded with Apotex and an unnamed company. If the allegations are proved, this is likely to have an adverse impact on the company. We had already booked out the stock in our note dated 15 November 2019.
  • Glenmark Pharmaceuticals

    29 Jun 2020 , 11:09AM Glenmark Q4FY2020 Result: Sturdy operating performance
  • Glenmark Pharmaceuticals launches COVID-19 drug after DCGI nod

    22 Jun 2020 , 11:28AM FabiFlu is the first oral Favipiravir-approved medication for the treatment of COVID-19
  • Glenmark

    22 Jun 2020 , 9:50AM DCGI approves restricted use of Favipiravir (Fabi Flu) to treat mild to moderate Covid 19 patients – Positive as the demand could surge with likely pick up in prescriptions
  • Glenmark Pharmaceuticals

    19 Jun 2020 , 12:36PM Gets final USFDA approval for Fingolimod Capsules - 0.5 mg, the generic version of Gilenya1 Capsules of Novartis Pharmaceuticals Corporation. As per IQVIA the sales for the generic medicine stood at $ 2.1 bn for the 12 month ending period as on April 2020. The approval is positive for the company considering the substantial size of opportunity in the US markets.
  • Glenmark Pharmaceuticals gets USFDA nod for Fingolimod capsules

    19 Jun 2020 , 11:56AM Glenmark Pharmaceuticals receives ANDA approval for Fingolimod Capsules, 0.5 mg
  • Glenmark Pharmaceuticals gets USFDA nod for Fingolimod capsules

    19 Jun 2020 , 11:55AM Glenmark Pharmaceuticals receives ANDA approval for Fingolimod Capsules, 0.5 mg
  • Sun Pharma, Glenmark

    11 Jun 2020 , 10:06AM Sun Pharma, Glenmark: As per media news, a coalition of 51 attorney generals in the US have filed an antitrust complaint in the federal court alleging that key individual executives and manufacturers of dermatological, generic drugs are engaged in a widespread conspiracy to artificially inflate and manipulate prices, reduce competition for generic drugs sold across the country. The complaint has mentions Taro, Teva, Glenmark amongst others. This is sentimentally negative for Glenmark and Sun Pharms as its subsidiary Taro, Teva are amongst mentioned in the conspiracy
  • Glenmark Pharmaceuticals

    27 May 2020 , 12:05PM Gets final approval from the USFDA for Chlorzoxazone Tablets USP – strength 375 mg and 750 mg. This marks Glenmark’s first ANDA approval out of the new North American manufacturing facility. As per IQVIA, the drug reported annual sales of USD 20.9 mn for 12 month ending March 2020. Positive as this could lead to improvement in the US business.
  • Glenmark Pharmaceuticals receives ANDA approval for Chlorzoxazone Tablets

    27 May 2020 , 10:04AM Glenmark's first ANDA approval out of their new US facility
  • Glenmark gets nod from Indian regulator to initiate study

    26 May 2020 , 10:48AM Glenmark to commence another new Phase 3 clinical trial on a combination of two anti-viral drugs
  • Glenmark Pharmaceuticals

    12 May 2020 , 11:45AM Glenmark has initiated Phase 3 clinical trials in India on Antiviral tablet Favipiravir, for which it received approval from India’s drug regulator DCGI in late April. Glenmark is the first company in India to initiate Phase 3 clinical trials on Favipiravir for COVID-19 patients in India. Favipiravir is a generic version of Avigan of Fujifilm Toyama Chemical Co. Japan, a subsidiary of Fujifilm Corporation. Glenmark has successfully developed the API and the formulations for the product through its inhouse R&D. If the trials are successful and the drug is approved by the regulators, it could offer potential growth opportunities for Glenmark.
  • Glenmark Pharmaceuticals

    11 May 2020 , 11:50AM As per media news, USFDA inspects the Monroe facility in US in last week and the inspection has ended with zero observations. The facility makes oral solids and injectable. Successful closure of the inspection with no observation is positive.
  • Glenmark introduces 3-in-1 inhaler therapy for COPD in India

    11 May 2020 , 10:53AM Glenmark introduces 3-in-1 inhaler therapy 'AIRZ-FF' for chronic obstructive pulmonary diseases
  • Glenmark receives approval from DGCI to conduct Clinical Trials in India

    30 Apr 2020 , 9:38AM Glenmark successfully developed the API and the formulations for the productthrough its in-house R&D team
  • Glenmark Pharmaceuticals gets USFDA tentative nod

    29 Apr 2020 , 10:48AM Glenmark Pharmaceuticals receives ANDA tentative approval for Dapagliflozin and Saxagliptin Tablets, 10 mg/5 mg
  • HUL to acquire VWash from Glenmark Pharmaceuticals

    24 Mar 2020 , 10:25AM Glenmark divests VWash, a female intimate hygiene wash, to Hindustan Unilever
  • Hindustan Unilever, Glenmark

    24 Mar 2020 , 9:39AM The company to acquire VWash from Glenmark Pharmaceuticals - positive from long term perspective as company enters into underpenetrated women hygiene product category
  • Glenmark

    23 Mar 2020 , 12:09PM US FDA has granted a tentative apporoval to Glenmark for Dapagliflozin Tablets, 5 mg and 10 mg. This is a generic version of Farxiga1 Tablets of AstraZeneca AB. According to IQVIATM sales data for the 12 month period ending January 2020, the Farxiga Tablets achieved annual sales of approximately $1.8 billion. Positive
  • Glenmark Pharmaceuticals gets USFDA nod for Dapagliflozin Tablets

    23 Mar 2020 , 10:05AM Glenmark Pharma receives USFDA tentative approval for Dapagliflozin Tablets
  • Glenmark, Hikma enter into an exclusive licensing agreement for commercializing Ryaltris

    27 Feb 2020 , 2:57PM Glenmark inks licensing pact with Hikma for commercialisation of nasal spray Ryaltris in US
  • Glenmark Pharmaceuticals

    26 Feb 2020 , 12:21PM As per media news, the US FDA has inspected the company’s plants at Aurangabad and Indore in between 17 February 2020 to 21 February 2020. The inspection ended with zero observations. Off the two plants, Indore plant caters to the US Markets. Successful closure of inspection with zero observations is positive
  • Glenmark Pharmaceuticals

    12 Feb 2020 , 11:24AM Board of Directors at the meeting scheduled on February 14, 2020, will consider and evaluate proposals for raising of funds either by issuance of bonds / debentures / non-convertible debt instruments or any other securities or any combination. The proceeds would be used for refinancing of current debt instruments - bonds/FCCBs/loans. This is likely to keep the debt levels elevated and stress the balance sheet position. We had recommended a book out on the stock citing high debt levels in our report dated 15 Nov 2019.
  • Glenmark Pharmaceuticals

    22 Jan 2020 , 11:30AM Has sold its gynaecology business to private equity firm True North backed Integrace Pharma, as Glenmark looks to cut down debt levels. The sale of the gynaecology business comes two years after it sold its orthopedic business to the same company. Glenmark would get a consideration of Rs 115 crore for four products of the portfolio that includes products like Dubagest, Mumfer and Fenza. These three products currently have sales of Rs 60 crore and are growing by 15%. As of September 2019 Glenmark’s debt on books stood at Rs 3265 cr, which is on the higher side. A repayment of Rs 115 crore, is unlikely to have any material impact on the total debt levels. We had closed our call on Glenmark and recommended a Book out citing high debt levels in our report dated 15th Nov 2019.
  • Cipla, Glenmark

    9 Jan 2020 , 12:42PM As per media news, the drug regulator NPPA (National Pharma Pricing Authority) has allowed both the companies to have an enhanced pricing for two of their respiratory (inhaler) products, on the grounds that these were ‘innovative’ from the other similar products available in the market. Positive read thru
  • Glenmark gets ANDA nod for Deferasirox Tablets for Oral Suspension

    7 Jan 2020 , 10:29AM Glenmark Pharmaceuticals receives USFDA nod for Deferasirox tablets, used to reduce chronic iron overload in patients
  • Glenmark gets product approval from Therapeutic Goods Administration

    20 Dec 2019 , 12:01PM Glenmark Pharmaceuticals announces product approval for Ryaltris in Australia
  • Glenmark Pharmaceuticals

    18 Dec 2019 , 2:50PM As per media reports, Glenmark Pharmaceuticals USA has voluntarily recalled all unexpired lots of its Ranitidine tablets and ceased distribution due to a possible presence of N-DMA impurities. Negative
  • Glenmark Pharma's Baddi unit gets GMP certificate

    16 Dec 2019 , 10:38AM Glenmark Pharma's Baddi unit gets Good Manufacturing Practice certificate by European regulator
  • Glenmark Pharma gets ANDA nod for extended-release tablets

    26 Nov 2019 , 10:18AM Glenmark Pharmaceuticals receives ANDA approval for Metformin Hydrochloride Extended-Release Tablets USP,500 mg and 1000 mg
  • Glenmark Pharma spurts after CLSA upgrades to 'buy'

    18 Nov 2019 , 12:46PM Glenmark Pharmaceuticals jumps by 16% to Rs. 350.25, after global brokerage CLSA upgrades the stock
  • Glenmark Pharmaceuticals

    15 Nov 2019 , 12:01PM Glenmark Q2FY2020 Result: Healthy performance; results beat estimates
  • Glenmark Pharma receives USFDA warning letter for Baddi facility

    7 Oct 2019 , 10:19AM USFDA inspection of Glenmark’s Baddi manufacturing facility in Himachal Pradesh
  • Glenmark

    1 Oct 2019 , 12:28PM Company receives approval from Russian Ministry of Healthcare to market Montlezir (Levocetirizine+Montelukast) film‐coated tablets; indicated for the treatment of seasonal and perennial allergic rhinitis –Montlezir is expected to be available in the Russian market in Q3 FY 2019‐20.
  • Glenmark goa plant concludes with 2 observations

    30 Sep 2019 , 11:01AM Glenmark: Company’s Goa plant inspected by the USFDA concluded with two observations – Sentimentally negative; Goa unit contributes ~ 30%.
  • Glenmark gets USFDA nod for Pimecrolimus topical cream

    30 Aug 2019 , 1:30PM Glenmark: Company gets USFDA approval for Pimecrolimus topical cream (gElidel Cream, of Bausch Health US, LLC), used to treat certain skin conditions such as eczema – Positive; gElidel had US sales of ~Rs 1425 crore (for 12 months ending July 2019).
  • Glenmark Pharmaceuticals gets ANDA nod for Fulvestrant Injection

    23 Aug 2019 , 12:10PM Glenmark Pharmaceuticals receives ANDA approval for Fulvestrant Injection, 250 mg/5 mL (50 mg/mL)
  • Glenmark Q1FY2020 Result

    14 Aug 2019 , 10:25AM Glenmark Q1FY2020 Result: Weak Numbers
  • Fitch assigns Glenmark’s Long-Term Issuer Default Rating

    12 Jul 2019 , 1:16PM Glenmark: Fitch assigns Glenmark’s Long-Term Issuer Default Rating (IDR) rating of 'BB' with stable outlook – Positive for Glenmark; The agency also affirmed the rating on Glenmark's USD200 million 4.50% senior unsecured notes due 2021 at 'BB' (stable).
  • Glenmark, Torrent sign licensing agreement for co‐marketing

    11 Jul 2019 , 1:08PM Glenamrk: Glenmark & Torrent sign licensing agreement for co‐marketing of Remogliflozin Etabonate (used to treat type-2 diabetes) in India – Neutral; Under the terms of non‐exclusive agreement, Glenmark will manufacture and supply Remogliflozin Etabonate while Torrent will market the drug under its own trademark in India.
  • Glenmark, Torrent ink pact for Remogliflozin Etabonate in India

    11 Jul 2019 , 10:31AM Glenmark, Torrent sign licensing agreement for co-marketing of Remogliflozin Etabonate in India
  • Glenmark Pharmaceuticals gets USFDA nod for Ranolazine tablets

    9 Jul 2019 , 10:53AM Glenmark Pharma gets USFDA nod for Ranolazine Tablet, used to treat heart related chest pain
  • Glenmark Pharma gets USFDA approval for generic tablets

    28 Jun 2019 , 10:45AM Glenmark Pharmaceuticals receives ANDA approval for Ezetimibe and Simvastatin Tablets
  • Glenmark to partner with Novartis for respiratory products

    24 Jun 2019 , 10:47AM Glenmark to partner with Novartis to promote, commercialize and distribute three respiratory products in Brazil
  • Glenmark gets tentative USFDA nod for Clindamycin

    20 Jun 2019 , 10:22AM Company receives tentative ANDA approval for Clindamycin Phosphate Foam, 1%
  • Glenmark Q4FY2019 performance below expectation

    30 May 2019 , 11:47AM Sales for the quarter grew by 12.4% to Rs 2563.5 crore; Operating profit grew by 11.3% to Rs 363.8 crore; OPM declined by 266 BPs to 14.2% and Adj. PAT reported decline of 2.2% to Rs 161.4 crore. Post management call (today 8.30 am ) we shall review our estimates and come out with detailed note. We currently have hold rating on the stock with PT under review.
  • Glenmark gets USFDA nod for Aspirin Capsules

    27 May 2019 , 11:23AM Glenmark Pharmaceuticals receives ANDA approval for Aspirin and Extended-Release Dipyridamole Capsules, 25 mg/200 mg
  • Glenmark gets USFDA nod for Solifenacin Succinate Tablets

    21 May 2019 , 11:28AM Glenmark: Company gets USFDA approval for Solifenacin Succinate Tablets (gVesicare) used to treat overactive bladder – Positive; gVesicare had annual sales of ~ Rs 6600 crore; Astellas & Teva are other players in the market.
  • Glenmark gets ANDA nod for Solifenacin Succinate Tablets

    21 May 2019 , 10:51AM Glenmark Pharmaceuticals receives ANDA approval for Solifenacin Succinate Tablets,5 mg and 10 mg
  • Glenmark gets USFDA nod for Esomeprazole Magnesium Delayed-Release Capsules

    14 May 2019 , 1:25PM Glenmark: Company gets USFDA approval for Esomeprazole Magnesium Delayed-Release Capsules (gNexium) – Positive for Glenmark; drug mentioned has US sales of ~Rs 2795 crore ; Alkem, Aurobindo, Amneal, Dr Reddy, Mylan, Sun Pharma & Torrent are other players in the market.
  • Glenmark Pharmaceuticals receives ANDA nod for Esomeprazole Magnesium

    14 May 2019 , 10:19AM Glenmark Pharma receives USFDA approval for Esomeprazole Magnesium Delayed-Release Capsules USP, 20 mg and 40 mg
  • Glenmark’s US subsidiary enters into co-promotion agreement with Otonomy

    3 May 2019 , 2:16PM Glenmark’s US subsidiary enters into co-promotion agreement with Otonomy, Inc (a biopharmaceutical company) dedicated to the development of innovative therapeutics for neurotology – Long term Positive; Financial terms for multi-year agreement is not disclosed; however, Glenmark will provide Otonomy an annual co-promotion fee and provide reimbursement of a proportion of product support expenses.
  • Glenmark launches novel, globally-researched anti-diabetes drug Remogliflozin in India

    30 Apr 2019 , 10:23AM Glenmark- Co launches novel, globally-researched anti-diabetes drug Remogliflozin (a patent-protected sodium glucose co-transporter-2 (SGLT2) inhibitor ) in India; indicated in the treatment of type-2 diabetes – Positive
  • Glenmark goa plant gets 5 observations from USFDA

    18 Mar 2019 , 10:48AM Glenmark: As per media reports, Company’s Goa plant gets 5 observations from USFDA – Negative read thru
  • Glenmark gets a USFDA nod for anti-bacterial gel

    15 Mar 2019 , 10:11AM Glenmark Pharmaceuticals receives ANDA approval for Clindamycin and Benzoyl Peroxide Gel, 1%/5%
  • Glenmark Pharma gets USFDA nod for Telmisartan & Hydrochlorothiazide tablets

    5 Mar 2019 , 10:21AM Glenmark Pharmaceuticals receives ANDA approval for Telmisartan and Hydrochlorothiazide Tablets USP
  • Glenmark gets USFDA nod for Clobetasol Propionate Foam

    18 Feb 2019 , 11:12AM Glenmark Pharmaceuticals receives ANDA approval for Clobetasol Propionate Foam, 0.05%
  • Glenmark Pharma signs agreement with Grandpharma

    6 Feb 2019 , 5:50PM Glenmark Pharmaceuticals enters into an Exclusive License Agreement with Grandpharma
  • Glenmark gets USFDA nod for Topiramate ER capsules

    24 Jan 2019 , 12:00PM Glenmark receives tentative ANDA approval for Topiramate Extended-Release Capsules
  • Glenmark gets tentative USFDA nod for cancer drug

    23 Jan 2019 , 11:01AM Glenmark gets tentative USFDA nod for generic of Zytiga Tablets
  • Glenmark enters into licensing agreement with Yuhan Corporation

    10 Jan 2019 , 11:23AM Glenmark enters into exclusive licensing agreement with Yuhan Corp for commercializing Glenmark's nasal spray Ryaltris in South Korea (Glenmark’s second regional licensing deal for Ryaltris ) – Positive; Glenmark will be responsible for manufacturing and supply of the product, while Yuhan will be responsible for regulatory filing and commercialization of Ryaltris in South Korea. Glenmark will receive an upfront payment, regulatory and commercial milestone payments and royalties from Yuhan for Ryaltris.
  • Glenmark enters into licensing agreement with Yuhan Corporation

    10 Jan 2019 , 11:20AM Glenmark will receive an upfront payment, regulatory and commercial milestone payments as well as royalties from Yuhan
  • Glenmark gets USFDA nod for Hydrocortisone Valerate Ointment

    17 Dec 2018 , 10:07AM Glenmark Pharmaceuticals receives ANDA approval for Hydrocortisone Valerate Ointment USP, 0.2%
  • Glenmark Pharma gets USFDA nod for Clobetasol Propionate Foam

    26 Nov 2018 , 11:19AM Glenmark Pharmaceuticals receives tentative ANDA approval for Clobetasol Propionate Foam, 0.05%
  • Glenmark Q2FY19 numbers better than expectation

    14 Nov 2018 , 10:07AM Glenmark Pharma Q2 net profit rises by 15% to Rs. 246.8 crore for the quarter ended September 2018
  • Glenmark Pharma to launch phase 1 trial in solid tumors

    9 Nov 2018 , 12:09PM Glenmark Pharmaceuticals announces decision to launch Phase 1 Trial in Solid Tumors for its CD38xCD3 Bispecific Antibody GBR 1342 Based on Human Translational Data
  • Glenmark introduce launch of Nourkrin in Russia

    1 Nov 2018 , 11:52AM Glenmark launches globally-renowned hair growth formula Nourkrin in Russia
  • Glenmark gets USFDA nod for generic Derma-Smoothe Topical Oil

    30 Oct 2018 , 12:46PM Glenmark Pharmaceuticals receives ANDA approval for Fluocinolone Acetonide Topical Oil, 0.01% (Scalp Oil)
  • Glenmark moves to dismiss lawsuit against in US Court

    19 Oct 2018 , 10:56AM Glenmark moves to dismiss lawsuit against it in US Court; Lawsuit pertains to company conspiring with Merck to delay production cholesterol drug Zetia – Stock to remain in focus.
  • Glenmark gets USFDA nod for Hydrocortisone Valerate cream

    15 Oct 2018 , 11:47AM Glenmark Pharmaceuticals receives ANDA approval for Hydrocortisone Valerate Cream USP, 0.2%
  • Glenmark completes transfer of API biz

    10 Oct 2018 , 12:08PM Glenmark: Completes transfer of API biz to Glenmark Life Sciences, a subsidiary; Company could look at monetizing its API business to reduce debt (FY18: Rs 4725 Crore) – Stock to remain in focus.
  • Glenmark gets USFDA nod

    17 Sep 2018 , 12:32PM Glenmark Pharmaceuticals receives USFDA approval for Estradiol Vaginal Inserts (generic version of VAGIFEM); product sales of ~ Rs 2050 crore – Positive for Glenmark
  • Business visibility and R&D monetisation key triggers

    11 Sep 2018 , 12:41PM Glenmark receives market authorisation in Germany for its generic version of Seretide Accuhaler
  • Glenmark arm secures German nod for asthma drug

    10 Sep 2018 , 11:53AM The drug, a generic version of a GlaxoSmithKline product, would be Gllenmark's first inhaler in German market.
  • Glenmark enters into exclusive licensing agreement

    29 Aug 2018 , 10:30AM Glenmark Pharmaceuticals enters into an exclusive licensing agreement to commercialize generic version of Boehringer Ingelheim’s Spiriva Handihaler (Tiotropium Bromide dry powder inhaler used in the treatment of chronic obstructive pulmonary disease (COPD)) in Western Europe; – Positive for Glenmark; Mentioned branded drug had ~Rs 5000 crore sales in EU
  • Glenmark enters into exclusive licensing agreement

    29 Aug 2018 , 10:28AM Glenmark enters into an exclusive licensing agreement to commercialize generic Tiotropium Bromide dry powder inhaler in Western Europe
  • Glenmark Q1 profit above estimates

    13 Aug 2018 , 12:00PM Glenmark Q1 net profit falls by 33.3% to Rs222.8 cr for the Quarter ended June 30, 2018 (YoY)
  • Glenmark Pharmaceuticals

    10 Aug 2018 , 11:52AM Glenmark Pharmaceuticals' as per media news, PE like True North eye about 20% in Glenmark API business for 1500-1800 crore, valuing API biz at around 8000 crore. Value unlocking , postive read-thru
  • Glenmark gets USFDA nod for Ryaltris

    8 Aug 2018 , 10:37AM Glenmark Pharmaceuticals gets USFDA acceptance of NDA for Ryaltris (nasal spray for treatment for seasonal allergic rhinitis); Target Action Date (TAD) for completion of the FDA review is March 21, 2019 – Positive read thru
  • Glenmark file appeal against CCI order before NCLAT

    17 Jul 2018 , 4:13PM Glenmark Pharma file an appeal against the order of the Competition Commission of India (CCI) before the National Company Law Appellate Tribunal
  • Glenmark Pharma buys stake in Zorg Labs

    17 Jul 2018 , 12:06PM Glenmark Pharma acquires 100% equity stake in Zorg Laboratories
  • Glenmark gets USFDA nod for facility in Monroe

    19 Jun 2018 , 11:03AM Glenmark announces that the USFDA provides its first supplemental ANDA nod for the company’s manufacturing facility in Monroe, North Carolina
  • Glenmark reports weak numbers

    30 May 2018 , 10:13AM We currently have a Hold rating with PT of Rs 600.
  • Glenmark gets USFDA nod for gWelchol

    21 May 2018 , 12:00PM Glenmark gets USFDA approval for Colesevelam Hydrochloride Tablets, 625 mg, the generic version of Welchol®1 Tablets, 625 mg, of Daiichi Sankyo Inc
  • Glenmark to present updated data on GBR 830 at IID

    10 May 2018 , 11:29AM Glenmark to present updated data on GBR 830 will be presented at the upcoming International Investigative Dermatology Meeting (IID) in Orlando, Florida
  • Glenmark initiates phase 2b clinical trial of GBR 830

    17 Apr 2018 , 10:30AM Glenmark initiates a Phase 2b clinical trial of GBR 830, a novel, investigational treatment for moderate- to-severe atopic dermatitis
  • Glenmark Pharma recalls over 1 lakh anti-inflammatory drug bottles

    6 Apr 2018 , 10:15AM Negative read through for Glenmark.
  • Glenmark enters into agreement with Helsinn

    5 Apr 2018 , 12:30PM Glenmark rises over 3% at Rs566.5, after entering into an exclusive licensing agreement with Helsinn Group to introduce AKYNZEO in India and Nepal
  • Glenmark presents new data on Ryaltris

    6 Mar 2018 , 10:38AM Positive read through for Glenmark as it presents new data on Ryaltris, an Investigational Product for the treatment of seasonal allergic rhinitis.
  • Glenmark enters into an exclusive agreement with Sam Chun Dang Pharm

    22 Feb 2018 , 10:31AM Positive read through for Glenmark as it enters Glenmark enters into an exclusive agreement with Sam Chun Dang Pharm. Co. Ltd. (SCD), to develop, manufacture and market a portfolio of ophthalmic products in the U.S. and Canada.
  • Glenmark reports disappointing performance in Q3FY18

    9 Feb 2018 , 12:40PM Sales for the quarter declined by 13% to Rs 2203.7 crore, mainly on account of 40% fall in US business (Q3FY2017 includes 180 day exclusivity sales for Zetia)
  • Glenmark gets USFDA approval for Norethindrone Acetate

    27 Dec 2017 , 11:41AM Positive read through for Glenmark; Negative for Lupin as it shall face competition
  • Glenmark to submit its first new drug application to FDA

    14 Dec 2017 , 2:43PM Glenmark announced that it met its primary clinical endpoint in a Phase 3 study evaluating the safety of Ryaltris.
  • Glenmark met primary clinical endpoint

    14 Dec 2017 , 9:54AM Glenmark announced that it met its primary clinical endpoint in a Phase 3 study evaluating the safety of Ryaltris.
  • Glenmark's Baddi Unit gets USFDA's Form 483

    29 Nov 2017 , 11:15AM Sentimentally Negative for Glenmark Pharma as USFDA issues Form 483 for Baddi Unit.
  • Glenmark falls on observations issued by USFDA

    28 Nov 2017 , 12:41PM Glenmark slips by 3% to Rs573.95, after the US drug regulator issued Form 483 with seven observations for its Baddi plant in Himachal Pradesh
  • Glenmark’s Baddi unit receives observations by USFDA

    28 Nov 2017 , 8:55AM Negative for Glenmark as the Baddi unit contributes ~ 10% to US sales (~ 5-7% total sales).
  • Glenmark gets USFDA nod for HAILEYTM Fe 1/20 tablets

    22 Nov 2017 , 11:37AM Glenmark announces receives final approval by the United States Food & Drug Administration (USFDA) for HAILEY Fe 1/20
  • Glenmark gets USFDA nod for generic version of oral contraceptive drug

    20 Nov 2017 , 9:28AM Positive news for Glenmark as it gets USFDA approval for generic version of Loestrin 24 Fe Tablets (market size of ~ Rs 625 crore), an oral contraceptive drug.
  • Glenmark Q2 results post weak operating performance

    6 Nov 2017 , 11:29AM Glenmark Pharmaceuticals (Glenmark Pharma) revenue grew 1.5% y-o-y to Rs. 2,256.6 crore for Q2FY18, while operating profit declined by 13.5% to Rs. 388.4 crore.
  • Glenmark profit beats expectation

    3 Nov 2017 , 1:04PM Sales for the quarter grew by 1.5% to Rs 2256.6 crore; US business reported decline of 5.7%.
  • Glenmark up as UK regulator renews Baddi unit license

    5 Oct 2017 , 12:30PM Glenmark rises over 4% to Rs626.65, on reports that UK drug regulator renews a manufacturing certificate for the company's Baddi unit
  • Glenmark gets USFDA nod for Desonide Ointment

    19 Sep 2017 , 10:12AM Glenmark gets USFDA approval for Desonide Ointment, used to treat the inflammation and itching caused by a number of skin conditions such as allergic reactions, eczema, and psoriasis – Positive for Glenmark
  • Glenmark gets USFDA nod for Triamcinolone

    23 Aug 2017 , 1:28PM Glenmark Pharmaceuticals announces that it has receive final approval from the US drug regulator for Triamcinolone Acetonide Ointment USP, 0.1%.
  • Glenmark gets USFDA nod for Acyclovir ointment, gZovirax

    2 Aug 2017 , 10:56AM Glenmark gets USFDA nod for Acyclovir ointment – Positive read thru.
  • Glenmark enters into agreement with Cyndea

    19 Jul 2017 , 12:27PM Glenmark Pharma rises over 2% to Rs707.1, after entering into a development, license, manufacture and commercial supply agreement with Cyndea Pharma S.L
  • Glenmark gains on USFDA nod for generic drug

    7 Jul 2017 , 12:38PM Glenmark Pharma rises by 2% to Rs667.65, after receiving ANDA approval for Amlodipine and Olmesartan Medoxomil Tablets
  • Glenmark gets tentative approval from USFDA for anti-diabetic drug

    14 Jun 2017 , 3:28PM Glenmark Pharma has been grant tentative approval by the United States Food & Drug Administration (USFDA) for Saxagliptin Tablets
  • Glenmark Pharma gets USFDA nod for generic drug; stk gains

    26 May 2017 , 12:22PM Glenmark Pharma rises by 3% to Rs628.7, after receiving final nod from the US drug regulator for Olmesartan Medoxomil Tablets, 5 mg, 20 mg and 40 mg.

Key fundamentals

Evaluate the intrinsic value of Glenmark Pharmaceuticals Ltd stock 

Name March-24 March-23 March-22 March-21 March-20
Assets 23627.854 21033.863 20408.936 18435.099 16800.027
Liabilities 23627.854 21033.863 20408.936 18435.099 16800.027
Equity 28.217 28.217 28.217 28.217 28.217
Gross Profit 1241.663 1472.767 1688.221 1890.341 1304.23
Net Profit 5167.291 1208.769 1997.789 1649.447 1354.548
Cash From Operating Activities -495.45 1474.063 1216.067 1243.417 1579.118
NPM(%) 65.48 14.7 24.53 21.79 20.17
Revenue 7891.119 8220.662 8141.581 7567.933 6712.631
Expenses 6649.456 6747.895 6453.36 5677.592 5408.401
ROE(%) 61.18 14.31 23.65 19.53 16.03

Shareholding Pattern

Corporate Action

XD-Date Dividend-Amount Dividend-% Dividend Yield(%GE) Price on that day
13 Sep 2024 2.5 250 0.17 1036
18 Sep 2023 2.5 250 0.17 624.3
12 Sep 2022 2.5 250 0.17 409.45
08 Sep 2021 2.5 250 0.17 607.6
17 Sep 2020 2.5 250 0.17 466.7
19 Sep 2019 2 200 0.17 544.6
19 Sep 2018 2 200 0.17 531.95
20 Sep 2017 2 200 0.17 759.55
03 Aug 2016 2 200 0.17 868.65
10 Sep 2015 2 200 0.17 875.3
10 Jul 2014 2 200 0.17 592.9
18 Jul 2013 2 200 0.17 521.35
19 Jul 2012 2 200 0.17 330.75
28 Jul 2011 0.4 40 0.17 284.7
16 Sep 2010 0.4 40 0.17 270.5
10 Sep 2009 0.4 40 0.17 229.8
07 Nov 2007 0.7 70 0.17 444.55
04 Jan 2007 0.8 40 0.17 569.75
07 Feb 2006 0.7 35 0.17 294.6
29 Apr 2005 0.7 35 0.17 287.95
31 Mar 2004 1.3 65 0.17 131.1
10 Jun 2003 6.5 65 0.17 236.8
12 Sep 2002 6 60 0.17 271.6
03 Sep 2001 4 40 0.17 106.5
0 80 0.17 270.05

Peers

Other companies within the same industry or sector that are comparable to Glenmark Pharmaceuticals Ltd

Company Price Price (% change) pe(x) EV/EBITDA(x) ROE(%) ROCE(%)
Albert David Ltd 810.15 -0.84 26.88 819.98 301.39 0.62
Lotus Eye Hospital and Institute Ltd 74.06 0.78 308.58 2987.91 14.01 0.68
Vaishali Pharma Ltd 12.85 -1.15 428.33 1540.08 2.76 0.00
Astec Lifesciences Ltd 701.25 -1.59 0.00 2817.34 -687.11 0.00

Company Info

1977 - The Company was incorporated on 18th, November, as "Glenmark Pharmaceuticals Private Limited" under the Companies Act, 1956, and became a deemed Public Company on July 1, 1990, then again became a private Company on September 27, 1990, the word Private was deleted on July 1, 1991 and became a Public Limited Company on January 12, 1996. - The Company is engaged in Research & Development, manufacturing and marketing of Pharmaceutical Formulations, domestically as well as overseas. The Company has two brands i.e. Ascoril Expectorant and Candid-B among the ORG top 300 leading Pharmaceutical brands in India. - The Company has a manufacturing facility at Satpur, Nasik. Besides manufacturing Oral Tablets, Liquids and Capsules it also equipped to manufacture Topicals - Creams, Lotions, Ointments and Powders. The plant has been awarded the WHO GMP Certificate indicative of the fact that the facilities and operations fully conform to the WHO requirements on quality standards. 1979 - The company entered the anti-fungal market, where competition was less due to the relatively smaller market size, by introducing Candid Cream. - The Company launched Candid Lotion. It also introduced Candid V-3, Candid V-1 and Candid V-Gel. 1981 - The Company launced Candid-B Cream, a topical anti-fungal steroid combination to target the hitherto untapped market. 1985 - Candid Mouth Paint was launched for oral thrush, targeted at Paediatricians. The Company launched Ascoril, a cough expectorant, and it is one of the most successful brands of the Company and is ranked 103rd as per ORG Aug'99-MAT. 1987 - The Company started a Research and Development Department at it's Nasik factory. 1990 - The Company launched Candiderma and it is now the number two brand in its segment with a market share of 6.6%. 1993 - The Company launched Candid Ear Drops. - The Company proposes to implement an ERP system, which is expected to improve operational efficiencies and assist in monitoring performance. The Company is creating a backbone for setting up the ERP system including purchase of requisite hardware and connectivity between Factories/Branches/Depots via leased lines and VSAT. - The Company proposes to implement the Sales & Distribution and Finance Module, followed by the Production and Material Resource Planning Module. 1995 - The Company launched Candid TV Suspension and Candidtral. - The Company has created an Employee Welfare Trust ("Trust") called "Glenmark Pharmaceuticals Limited Employee Welfare Trust" to implement the Employee Stock Option Plan. 1997 - The Company established a Cardiac Center at Dadar, in Mumbai. - Glenmark proposes to set up a drug discovery center in the Thane Belapur area (suburb of Mumbai). 1999 - The Company proposes to launch line extensions and new products to expand its product basket in the existing segments and also capitalise on its doctor penetration. The Company also proposes to establish a subsidiary in Canada, to penetrate the market. - The Company allotted 1,75,000 warrants to the Trust for cash on September 20th, at Rs 1.0 per warrant. - Altacef, Suprocin, Suprocin B, Scalpe and Elovera were launched during the year and has been the most successful product by the Company, recording high growth. - The company is coming out with a public issue of 26,70,000 equity shares of Rs. 10 each for cash at a premium of Rs. 190 per share to fund its proposed expansion plan. The issue will open for subscription on December 10. - The company is setting up a soft gel capsule manufacturing facility at Goa at a total cost of Rs 19.4 crore for exports to US and a research and development centre in Mumbai at a cost of over Rs 11 crore. - Glenmark Pharmaceuticals, a Mumbai-based company, will be the first to test the waters from Industrial sector, viz., pharmaceuticals sector, while many other companies are waiting in the wing. 2000 - The Glenmark Pharmaceutical scrip opened its innings on the Bombay Stock Exchange at Rs 550, a whopping 175 per cent increase over the issue price of Rs 200 (including a premium of Rs 190) per share. - The Company has entered into a strategic alliance with Haller Group (HG) of Brazil. - The Company is to issue 30,00,000 No. of equity shares of Rs 10 each on private placement to finance the R&D and US FDA projects as also several opportunities for acquisitions and alliances to achieve higher growth. - The Company is to increase the borrowing powers from Rs 25 crores to Rs 150 crores. - The Company has acquired three brands, viz. Alex, Flucort and Sensur from Lyka Labs Ltd. 2001 - The board proposes to issue, through private placement, 40,00,000 redeemable cumulative non-convertible preference shares of Rs 100 each bearing dividend of not less than 9 per cent per annum and not exceeding 10.50 per cent per annum. 2002 -Establishes 'Proof of concept' in animal for their anti-diabetic / anti -obesity agent GRC-1087 which is a highly potent and selective human beta 3 andrnoceptor agoinst. -Company co-opted 3 directors Mr. Rajiv V Desai, Mr A S Mohanty, and Mr Sameer Paigankar in its board. -Dr Robin Pinto resigns as the director on the board of the company. -CDC Financial Services Ltd acquires 25,00,000 convertible debentures of the company of Rs.100 each. 2003 -Members approve for the disinvestment of company's right, title and interest in Assets & immovable property relating to manufacturing facilities located in at Verna, Goa. -Forays into the US generic markets and has roped in a former vice-president of Dr. Reddy's Laboratories to run the activities. -Declares interim dividend of 65% on the paid up equity capital of the company. -Directors allot 21000 equity shares to employees on ESOP scheme of the company. -Enters into a marketing arrangement with Philadaphia based Lannett Company, US to market the ANDA's . -Board approves for the sub division of equity shares from Rs.10 to Rs.2 per share. -Submitts Initial Drug Master File on Amiodarone -Fire breaks out at Kurkum factory and manufacturing operations have been suspended. -The Company ties up with Apotex, Canada, for the supply of a new generation bulk drug in cardiac segment. -Board approves Conversion of Debentures into equity shares at a price of Rs 305.42 per share, resulting in allotment of 818557 equity shares . 2004 -Glenmark Pharmaceuticals Inc, USA signs Development & Marketing Agreement with KV Pharmaceutical Company. -Glenmark Pharmaceuticals has acquired Laboratories Klinger in Brazil for $5.2m through its wholly owned subsidiary in Brazil, Glenmark Farmaceuitca -Glenmark Pharmaceuticals Ltd acquires two FDA approved products from Clonmel Healthcare Ltd -Glenmark Pharmaceuticals SA (Switzerland), a wholly owned subsidiary of Glenmark Pharmaceuticals India (GPL), has entered into a collaboration agreement with Forest Laboratories Inc, USA, for the development and commercialisation of PDE4 (phosphodiesterase 4) inhibitor GRC 3886 for chronic obstructive pulmonary disorder (COPD) and asthma 2005 -Glenmark forges alliance with 2 US firms to sell products in US -Glenmark Pharmaceuticals & Teijin Pharma announces Collaboration Agreement on PDE4 inhibitor GRC 3886 -Glenmark Pharmaceuticals Ltd has announced that Glenmark Pharmaceuticals SA (GPSA), a wholly owned Swiss subsidiary of the Company, acquired an Argentine marketing company Servycal S A (Servycal) for an undisclosed consideration -Glenmark Pharmaceuticals signs development & marketing agreement with InvaGen -Glenmark Pharmaceuticals has given the Bonus in the Ratio of 1:1 2006 -Glenmark Pharmaceuticals - Glenmark USA acquires exclusive marketing rights to 3 additional generic products -Glenmark & Paul Capital Partners Sign Unique Royalty Deal for USD 27 mn to build US Generic Dermatology Portfolio -Glenmark Pharmaceuticals US subsidiary inks agreement with Lehigh -Glenmark Pharmceuticals to acquire generic company in Europe -Glenmark Pharmaceuticals joins hands with US firm 2007 - Glenmark Pharmaceuticals received tentative US FDA approval for its ANDA for Topiramte Tablet - Glenmark receives MHRA, UK approval for its state-of-the art semi-solids manufacturing plant at Baddi - In a $350 million deal with US based Eli Lily, Glenmark Pharmaceuticals has out-licensed GRC 6211 and a few other smaller molecules with potential to treat pain. Glenmark has received an upfront payment of $45 million from Eli Lily and going forward the companies will share the benefits from the sales when it hits the market in 2012. - The Company has splits its face value from Rs2/- to Rs1/-. 2008 -Glenmark Pharmaceuticals - Glenmark launches Nabumetone & Hydroxyzine Hydrochloride Table -Glenmark Pharmaceuticals launches Clobetasol from its niche dermatology pipeline -Glenmark Generics launches trandolapril tablets -Glenmark's subsidiary received USFDA approval for Betamethasone Dipropionate Cream, 0.05% (Augmented) 2009 - Glenmark Pharmaceuticals Ltd has informed that Mr. M J Mendonza, has joined the Company as Vice President - Legal & Company Secretary with effect from February 06, 2009. - Glenmark Generics Limited (GGL) has received ANDA approval from the United States Food and Drug Administration (U.S. FDA) for Alclometasone Dipropionate Cream, 0.05% and will commence marketing and distribution of this product in the U.S. market immediately. - Glenmark Pharmaceuticals Ltd has appointed Mr. D R Mehta as Additional Director of the Company. The company has also appointed Mrs. B E Saldanha as Additional Director of the Company. - Glenmark Generics Limited's (GGL) US subsidiary has received ANDA approval from the United States Food and Drug Administration (U.S. FDA) for Verapamil 240mg Extended Release tablet s and will immediately commence marketing and distribution in the U.S. market. 2010 - Glenmark Pharmaceuticals Ltd has entered into a settlement and license agreement with Sepracor Inc to market generic Eszopiclone tablets. 2011 - Glenmark wins Two Prestigious Global Recognitions at SCRIP Awards 2011. - Glenmark exercises its purchase option election with respect to its Royalty agreement with Paul Capital Partner's Royalty Fund ("Paul Capital"). - Glenmark forays into Cosmeceutical Segment. - GBR 500 Deal receives clearance from Hart - Scott- Rodino Anti trust Improvements Act, USA. 2012 - Forest Laboratories and Glenmark Sign Development Agreement for Worldwide Collaboration on Novel Agents to treat Chronic Inflammatory Conditions. - Glenmark Generics announces the settlement of Paragraph IV litigation with Janssen Pharmaceuticals, Inc. - Glenmark Generics receives tentative approval for zolmitriptan orally disintegrating tablets. - The International Centre for Dispute Resolution ruled in favor of Glenmark on arbitration claim against Napo. - Glenmark Pharmaceuticals Ltd has informed BSE regarding a Press Release dated May 16, 2012 titled "Glenmark Generics receives tentative approval for zolmitriptan orally disintegrating tablets from the U. S. FDA". 2013 -Glenmark announces launch of Hydrocortisone Butyrate cream in the US. -Glenmark announces a new Discovery and the Initiation of IND enabling studies of a novel monoclonal antibody targeting OX40. -USFDA approves Crofelemer 125 mg delayed-release tablets for the symptomatic relief of diarrhea in patients with HIV/AIDS on anti-retroviral therapy (ART). -Glenmark Generics receives ANDA approval for Mupirocin Calcium Cream USP 2%. -Atovaquone Prognanil (Malarone) patent revoked & Glenmark launches first UK generic. -Glenmark discovers IND enabling studies of a novel monoclonal antibody. 2014 -Glenmark merge its subsidiaries i.e. Glenmark Generics Ltd. ("GGL") and Glenmark Access Ltd. ("GAL") with GPL. -Glenmark enters Oncology with the Discovery and the Initiation of IND enabling Studies of an innovative bispecific Antibody. -Glenmark Pharmaceuticals inaugurates new Antibody Manufacturing Facility in La Chaux-de-Fonds, Switzerland. -US Food & Drug Administration (US FDA) has granted Glenmark its final acceptance for abbreviated new drug approval (ANDA) to the company. -Glenmark Pharma receives $5 mn from Sanofi as milestone payment from Sanofi on a collaboration of its VLA2 (alpha2-beta l) integrin monoclonal antibody. -Glenmark Generics gets USFDA nod for skin infection cream. 2015 -Glenmark Pharmaceuticals Ltd - "Glenmark announces approval and launch of Ashlyna TM Extended - Cycle Oral Contraceptive Tablets in the US". -Glenmark Pharmaceuticals Ltd - "Glenmark announces approval and launch of Trandolapril & Verapamil Hydrochloride (HCI) Extended Release Tablets in the US" -Glenmark Pharma gets US FDA nod for Salmecort MDI Inhaler in Russia -The Cabinet Committee on Economic Affairs (CCEA) headed by PM has approved the foreign investment proposals of two pharma majors Glenmark Pharmaceuticals and Aurobindo Pharma worth Rs 4,187 crore, -Glenmark Pharmaceuticals Ltd. has certified approving the Scheme of Arrangement of Glenmark Generics Ltd. and Glenmark Access Ltd. with Glenmark Pharmaceuticals Ltd. -Glenmark announces Strategic Development & Licensing Agreement with Celon, Poland for generic Seretide Accuhalerr in Europe -Glenmark Pharmaceuticals receives tentative ANDA approval for Lacosamide Tablets, 50 mg, 100 mg, 150 mg and 200 mg -Glenmark Pharmaceuticals receives ANDA approval for Clotrimazole and Betamethasone Dipropionate Cream USP, 1% | 0.05% -Glenmark Pharmaceuticals has entered into a settlement agreement with Forest Laboratories, LLC, Forest Laboratories Holdings, Ltd., and Royalty Pharma 2016 -Glenmark Pharma gets tentative FDA nod for anti-arrhythmic drug -Glenmark Pharma discovers new molecule -Glenmark gets USFDA nod for cancer treatment drug -Glenmark receives approval for Raloxifene tablets -Glenmark gets 3 observations from USFDA for Indore plant -Glenmark bags approval for Triamcinolone Acetonide Ointment -Glenmark Launches First and Only Generic Version of Zetiar in the United States -Glemark Pharma bags approval for Tretinoin Capsules 2017 -Glenmark Pharmaceuticals and Evestra, Inc. Announce Partnership Agreement for Generic NuvaRingr. -Glenmark Pharma enters into agreement with APC Therapeutics Inc. -Glenmark Pharmaceuticals Enters Exclusive Agreement with Cyndea Pharma S.L. for Generic Soft-Gelatin Capsule Drug Products". -Glenmark Pharma launches nicotine substitute gum. 2018 -Glenmark launches globally-renowned hair growth formula Nourkrinr in Russia -Glenmark launches the biosimilar of Adalimumab in India -Glenmark Pharmaceuticals Enters Exclusive Collaboration Agreement with SCD Pharmaceuticals, South Korea, for Ophthalmic Solution Products -Glenmark announces successful launch of generic Seretider Accuhalerr in Denmark -Glenmark Pharmaceuticals is collaboration with True North for its orthopaedic and pain management business in India 2019 -Glenmark Pharmaceuticals has Licensing Agreement with Yuhan Corporation for commercializing Investigational Seasonal Allergic Rhinitis Nasal Spray Ryaltris in South Korea -Glenmark & Torrent Sign Licensing Agreement For Co-Marketing Of Remogliflozin Etabonate In India -Glenmark Pharmaceuticals secures prestigious Dow Jones Sustainability Emerging Markets Index for the second year in a row 2020 -Glenmark becomes the first company to launch Remogliflozin Vildagliptin fixed dose combination for adults with Type 2 Diabetes -Glenmark introduces NINDANIB (Nintedanib) for the treatment of Pulmonary Fibrosis in India -Glenmark introduces higher strength (400 mg) of FabiFlur to reduce pill burden of COVID-19 treatment -Glenmark Pharmaceuticals has got approval from the US health regulator for Deferasirox tablets for oral suspension -Glenmark pledges 50 lakh meals for undernourished children, pregnant women and daily wage earners amidst COVID-19 pandemic -Glenmark Pharmaceuticals and Hikma enter into an Exclusive Licensing Agreement for commercializing Ryaltris Seasonal Allergic Rhinitis Nasal Spray in the US 2021 -Glenmark introduces was awarded International Safety Award 2021 -Glenmark introduces was awarded Environmental, Social and Governance Summit & Awards 2021 -Glenmark Pharmaceuticals launches Rufinamide Tablets USP, 200 mg and 400 mg -Glenmark launches Ryaltrisr nasal spray at an affordable price in India 2022 -Glenmark gets US drug regulator's nod for high BP medicine. -Glenmark gets US FDA approval for Nicardipine Hydrochloride capsules. -Glenmark Pharma gets ANDA approval for generic birth control drug. -Glenmark receives the 'India Pharma Innovation of the Year' Award from the Government of India. -Glenmark is the first company to launch in India a Triple FDC of Teneligliptin Pioglitazone Metformin for Adults with Type 2 Diabetes & High Insulin Resistance. -Glenmark Pharmaceuticals launches Fingolimod Capsules, 0.5 mg in the US. 2023 -"Glenmark Pharmaceuticals launches Bumetanide Injection USP, 1 mg/4 mL (0.25mg/mL) Single-Dose Vials and 2.5 mg/10 mL (0.25 mg/mL) Multi-Dose Vials". 2024 -Glenmark Pharmaceuticals eceived approval from the US health regulator to market a generic medication to treat conditions caused by too much acid production in the stomach. -Glenmark Pharmaceuticals Inc. USA launches Lacosamide Oral Solution, 10 mg/mL. -Glenmark Pharmaceuticals Inc. USA launches Travoprost Ophthalmic Solution USP, 0.004% . -Glenmark Pharmaceuticals receives ANDA approval for Topiramate Capsules USP, 15 mg and 25 mg -Glenmark and BeiGene Enter into an Agreement for Marketing and Distribution of Tislelizumab and Zanubrutinib in India.

1977 - The Company was incorporated on 18th, November, as "Glenmark Pharmaceuticals Private Limited" under the Companies Act, 1956, and became a deemed Public Company on July 1, 1990, then again became a private Company on September 27, 1990, the word Private was deleted on July 1, 1991 and became a Public Limited Company on January 12, 1996. - The Company is engaged in Research & Development, manufacturing and marketing of Pharmaceutical Formulations, domestically as well as overseas. The Company has two brands i.e. Ascoril Expectorant and Candid-B among the ORG top 300 leading Pharmaceutical brands in India. - The Company has a manufacturing facility at Satpur, Nasik. Besides manufacturing Oral Tablets, Liquids and Capsules it also equipped to manufacture Topicals - Creams, Lotions, Ointments and Powders. The plant has been awarded the WHO GMP Certificate indicative of the fact that the facilities and operations fully conform to the WHO requirements on quality standards. 1979 - The company entered the anti-fungal market, where competition was less due to the relatively smaller market size, by introducing Candid Cream. - The Company launched Candid Lotion. It also introduced Candid V-3, Candid V-1 and Candid V-Gel. 1981 - The Company launced Candid-B Cream, a topical anti-fungal steroid combination to target the hitherto untapped market. 1985 - Candid Mouth Paint was launched for oral thrush, targeted at Paediatricians. The Company launched Ascoril, a cough expectorant, and it is one of the most successful brands of the Company and is ranked 103rd as per ORG Aug'99-MAT. 1987 - The Company started a Research and Development Department at it's Nasik factory. 1990 - The Company launched Candiderma and it is now the number two brand in its segment with a market share of 6.6%. 1993 - The Company launched Candid Ear Drops. - The Company proposes to implement an ERP system, which is expected to improve operational efficiencies and assist in monitoring performance. The Company is creating a backbone for setting up the ERP system including purchase of requisite hardware and connectivity between Factories/Branches/Depots via leased lines and VSAT. - The Company proposes to implement the Sales & Distribution and Finance Module, followed by the Production and Material Resource Planning Module. 1995 - The Company launched Candid TV Suspension and Candidtral. - The Company has created an Employee Welfare Trust ("Trust") called "Glenmark Pharmaceuticals Limited Employee Welfare Trust" to implement the Employee Stock Option Plan. 1997 - The Company established a Cardiac Center at Dadar, in Mumbai. - Glenmark proposes to set up a drug discovery center in the Thane Belapur area (suburb of Mumbai). 1999 - The Company proposes to launch line extensions and new products to expand its product basket in the existing segments and also capitalise on its doctor penetration. The Company also proposes to establish a subsidiary in Canada, to penetrate the market. - The Company allotted 1,75,000 warrants to the Trust for cash on September 20th, at Rs 1.0 per warrant. - Altacef, Suprocin, Suprocin B, Scalpe and Elovera were launched during the year and has been the most successful product by the Company, recording high growth. - The company is coming out with a public issue of 26,70,000 equity shares of Rs. 10 each for cash at a premium of Rs. 190 per share to fund its proposed expansion plan. The issue will open for subscription on December 10. - The company is setting up a soft gel capsule manufacturing facility at Goa at a total cost of Rs 19.4 crore for exports to US and a research and development centre in Mumbai at a cost of over Rs 11 crore. - Glenmark Pharmaceuticals, a Mumbai-based company, will be the first to test the waters from Industrial sector, viz., pharmaceuticals sector, while many other companies are waiting in the wing. 2000 - The Glenmark Pharmaceutical scrip opened its innings on the Bombay Stock Exchange at Rs 550, a whopping 175 per cent increase over the issue price of Rs 200 (including a premium of Rs 190) per share. - The Company has entered into a strategic alliance with Haller Group (HG) of Brazil. - The Company is to issue 30,00,000 No. of equity shares of Rs 10 each on private placement to finance the R&D and US FDA projects as also several opportunities for acquisitions and alliances to achieve higher growth. - The Company is to increase the borrowing powers from Rs 25 crores to Rs 150 crores. - The Company has acquired three brands, viz. Alex, Flucort and Sensur from Lyka Labs Ltd. 2001 - The board proposes to issue, through private placement, 40,00,000 redeemable cumulative non-convertible preference shares of Rs 100 each bearing dividend of not less than 9 per cent per annum and not exceeding 10.50 per cent per annum. 2002 -Establishes 'Proof of concept' in animal for their anti-diabetic / anti -obesity agent GRC-1087 which is a highly potent and selective human beta 3 andrnoceptor agoinst. -Company co-opted 3 directors Mr. Rajiv V Desai, Mr A S Mohanty, and Mr Sameer Paigankar in its board. -Dr Robin Pinto resigns as the director on the board of the company. -CDC Financial Services Ltd acquires 25,00,000 convertible debentures of the company of Rs.100 each. 2003 -Members approve for the disinvestment of company's right, title and interest in Assets & immovable property relating to manufacturing facilities located in at Verna, Goa. -Forays into the US generic markets and has roped in a former vice-president of Dr. Reddy's Laboratories to run the activities. -Declares interim dividend of 65% on the paid up equity capital of the company. -Directors allot 21000 equity shares to employees on ESOP scheme of the company. -Enters into a marketing arrangement with Philadaphia based Lannett Company, US to market the ANDA's . -Board approves for the sub division of equity shares from Rs.10 to Rs.2 per share. -Submitts Initial Drug Master File on Amiodarone -Fire breaks out at Kurkum factory and manufacturing operations have been suspended. -The Company ties up with Apotex, Canada, for the supply of a new generation bulk drug in cardiac segment. -Board approves Conversion of Debentures into equity shares at a price of Rs 305.42 per share, resulting in allotment of 818557 equity shares . 2004 -Glenmark Pharmaceuticals Inc, USA signs Development & Marketing Agreement with KV Pharmaceutical Company. -Glenmark Pharmaceuticals has acquired Laboratories Klinger in Brazil for $5.2m through its wholly owned subsidiary in Brazil, Glenmark Farmaceuitca -Glenmark Pharmaceuticals Ltd acquires two FDA approved products from Clonmel Healthcare Ltd -Glenmark Pharmaceuticals SA (Switzerland), a wholly owned subsidiary of Glenmark Pharmaceuticals India (GPL), has entered into a collaboration agreement with Forest Laboratories Inc, USA, for the development and commercialisation of PDE4 (phosphodiesterase 4) inhibitor GRC 3886 for chronic obstructive pulmonary disorder (COPD) and asthma 2005 -Glenmark forges alliance with 2 US firms to sell products in US -Glenmark Pharmaceuticals & Teijin Pharma announces Collaboration Agreement on PDE4 inhibitor GRC 3886 -Glenmark Pharmaceuticals Ltd has announced that Glenmark Pharmaceuticals SA (GPSA), a wholly owned Swiss subsidiary of the Company, acquired an Argentine marketing company Servycal S A (Servycal) for an undisclosed consideration -Glenmark Pharmaceuticals signs development & marketing agreement with InvaGen -Glenmark Pharmaceuticals has given the Bonus in the Ratio of 1:1 2006 -Glenmark Pharmaceuticals - Glenmark USA acquires exclusive marketing rights to 3 additional generic products -Glenmark & Paul Capital Partners Sign Unique Royalty Deal for USD 27 mn to build US Generic Dermatology Portfolio -Glenmark Pharmaceuticals US subsidiary inks agreement with Lehigh -Glenmark Pharmceuticals to acquire generic company in Europe -Glenmark Pharmaceuticals joins hands with US firm 2007 - Glenmark Pharmaceuticals received tentative US FDA approval for its ANDA for Topiramte Tablet - Glenmark receives MHRA, UK approval for its state-of-the art semi-solids manufacturing plant at Baddi - In a $350 million deal with US based Eli Lily, Glenmark Pharmaceuticals has out-licensed GRC 6211 and a few other smaller molecules with potential to treat pain. Glenmark has received an upfront payment of $45 million from Eli Lily and going forward the companies will share the benefits from the sales when it hits the market in 2012. - The Company has splits its face value from Rs2/- to Rs1/-. 2008 -Glenmark Pharmaceuticals - Glenmark launches Nabumetone & Hydroxyzine Hydrochloride Table -Glenmark Pharmaceuticals launches Clobetasol from its niche dermatology pipeline -Glenmark Generics launches trandolapril tablets -Glenmark's subsidiary received USFDA approval for Betamethasone Dipropionate Cream, 0.05% (Augmented) 2009 - Glenmark Pharmaceuticals Ltd has informed that Mr. M J Mendonza, has joined the Company as Vice President - Legal & Company Secretary with effect from February 06, 2009. - Glenmark Generics Limited (GGL) has received ANDA approval from the United States Food and Drug Administration (U.S. FDA) for Alclometasone Dipropionate Cream, 0.05% and will commence marketing and distribution of this product in the U.S. market immediately. - Glenmark Pharmaceuticals Ltd has appointed Mr. D R Mehta as Additional Director of the Company. The company has also appointed Mrs. B E Saldanha as Additional Director of the Company. - Glenmark Generics Limited's (GGL) US subsidiary has received ANDA approval from the United States Food and Drug Administration (U.S. FDA) for Verapamil 240mg Extended Release tablet s and will immediately commence marketing and distribution in the U.S. market. 2010 - Glenmark Pharmaceuticals Ltd has entered into a settlement and license agreement with Sepracor Inc to market generic Eszopiclone tablets. 2011 - Glenmark wins Two Prestigious Global Recognitions at SCRIP Awards 2011. - Glenmark exercises its purchase option election with respect to its Royalty agreement with Paul Capital Partner's Royalty Fund ("Paul Capital"). - Glenmark forays into Cosmeceutical Segment. - GBR 500 Deal receives clearance from Hart - Scott- Rodino Anti trust Improvements Act, USA. 2012 - Forest Laboratories and Glenmark Sign Development Agreement for Worldwide Collaboration on Novel Agents to treat Chronic Inflammatory Conditions. - Glenmark Generics announces the settlement of Paragraph IV litigation with Janssen Pharmaceuticals, Inc. - Glenmark Generics receives tentative approval for zolmitriptan orally disintegrating tablets. - The International Centre for Dispute Resolution ruled in favor of Glenmark on arbitration claim against Napo. - Glenmark Pharmaceuticals Ltd has informed BSE regarding a Press Release dated May 16, 2012 titled "Glenmark Generics receives tentative approval for zolmitriptan orally disintegrating tablets from the U. S. FDA". 2013 -Glenmark announces launch of Hydrocortisone Butyrate cream in the US. -Glenmark announces a new Discovery and the Initiation of IND enabling studies of a novel monoclonal antibody targeting OX40. -USFDA approves Crofelemer 125 mg delayed-release tablets for the symptomatic relief of diarrhea in patients with HIV/AIDS on anti-retroviral therapy (ART). -Glenmark Generics receives ANDA approval for Mupirocin Calcium Cream USP 2%. -Atovaquone Prognanil (Malarone) patent revoked & Glenmark launches first UK generic. -Glenmark discovers IND enabling studies of a novel monoclonal antibody. 2014 -Glenmark merge its subsidiaries i.e. Glenmark Generics Ltd. ("GGL") and Glenmark Access Ltd. ("GAL") with GPL. -Glenmark enters Oncology with the Discovery and the Initiation of IND enabling Studies of an innovative bispecific Antibody. -Glenmark Pharmaceuticals inaugurates new Antibody Manufacturing Facility in La Chaux-de-Fonds, Switzerland. -US Food & Drug Administration (US FDA) has granted Glenmark its final acceptance for abbreviated new drug approval (ANDA) to the company. -Glenmark Pharma receives $5 mn from Sanofi as milestone payment from Sanofi on a collaboration of its VLA2 (alpha2-beta l) integrin monoclonal antibody. -Glenmark Generics gets USFDA nod for skin infection cream. 2015 -Glenmark Pharmaceuticals Ltd - "Glenmark announces approval and launch of Ashlyna TM Extended - Cycle Oral Contraceptive Tablets in the US". -Glenmark Pharmaceuticals Ltd - "Glenmark announces approval and launch of Trandolapril & Verapamil Hydrochloride (HCI) Extended Release Tablets in the US" -Glenmark Pharma gets US FDA nod for Salmecort MDI Inhaler in Russia -The Cabinet Committee on Economic Affairs (CCEA) headed by PM has approved the foreign investment proposals of two pharma majors Glenmark Pharmaceuticals and Aurobindo Pharma worth Rs 4,187 crore, -Glenmark Pharmaceuticals Ltd. has certified approving the Scheme of Arrangement of Glenmark Generics Ltd. and Glenmark Access Ltd. with Glenmark Pharmaceuticals Ltd. -Glenmark announces Strategic Development & Licensing Agreement with Celon, Poland for generic Seretide Accuhalerr in Europe -Glenmark Pharmaceuticals receives tentative ANDA approval for Lacosamide Tablets, 50 mg, 100 mg, 150 mg and 200 mg -Glenmark Pharmaceuticals receives ANDA approval for Clotrimazole and Betamethasone Dipropionate Cream USP, 1% | 0.05% -Glenmark Pharmaceuticals has entered into a settlement agreement with Forest Laboratories, LLC, Forest Laboratories Holdings, Ltd., and Royalty Pharma 2016 -Glenmark Pharma gets tentative FDA nod for anti-arrhythmic drug -Glenmark Pharma discovers new molecule -Glenmark gets USFDA nod for cancer treatment drug -Glenmark receives approval for Raloxifene tablets -Glenmark gets 3 observations from USFDA for Indore plant -Glenmark bags approval for Triamcinolone Acetonide Ointment -Glenmark Launches First and Only Generic Version of Zetiar in the United States -Glemark Pharma bags approval for Tretinoin Capsules 2017 -Glenmark Pharmaceuticals and Evestra, Inc. Announce Partnership Agreement for Generic NuvaRingr. -Glenmark Pharma enters into agreement with APC Therapeutics Inc. -Glenmark Pharmaceuticals Enters Exclusive Agreement with Cyndea Pharma S.L. for Generic Soft-Gelatin Capsule Drug Products". -Glenmark Pharma launches nicotine substitute gum. 2018 -Glenmark launches globally-renowned hair growth formula Nourkrinr in Russia -Glenmark launches the biosimilar of Adalimumab in India -Glenmark Pharmaceuticals Enters Exclusive Collaboration Agreement with SCD Pharmaceuticals, South Korea, for Ophthalmic Solution Products -Glenmark announces successful launch of generic Seretider Accuhalerr in Denmark -Glenmark Pharmaceuticals is collaboration with True North for its orthopaedic and pain management business in India 2019 -Glenmark Pharmaceuticals has Licensing Agreement with Yuhan Corporation for commercializing Investigational Seasonal Allergic Rhinitis Nasal Spray Ryaltris in South Korea -Glenmark & Torrent Sign Licensing Agreement For Co-Marketing Of Remogliflozin Etabonate In India -Glenmark Pharmaceuticals secures prestigious Dow Jones Sustainability Emerging Markets Index for the second year in a row 2020 -Glenmark becomes the first company to launch Remogliflozin Vildagliptin fixed dose combination for adults with Type 2 Diabetes -Glenmark introduces NINDANIB (Nintedanib) for the treatment of Pulmonary Fibrosis in India -Glenmark introduces higher strength (400 mg) of FabiFlur to reduce pill burden of COVID-19 treatment -Glenmark Pharmaceuticals has got approval from the US health regulator for Deferasirox tablets for oral suspension -Glenmark pledges 50 lakh meals for undernourished children, pregnant women and daily wage earners amidst COVID-19 pandemic -Glenmark Pharmaceuticals and Hikma enter into an Exclusive Licensing Agreement for commercializing Ryaltris Seasonal Allergic Rhinitis Nasal Spray in the US 2021 -Glenmark introduces was awarded International Safety Award 2021 -Glenmark introduces was awarded Environmental, Social and Governance Summit & Awards 2021 -Glenmark Pharmaceuticals launches Rufinamide Tablets USP, 200 mg and 400 mg -Glenmark launches Ryaltrisr nasal spray at an affordable price in India 2022 -Glenmark gets US drug regulator's nod for high BP medicine. -Glenmark gets US FDA approval for Nicardipine Hydrochloride capsules. -Glenmark Pharma gets ANDA approval for generic birth control drug. -Glenmark receives the 'India Pharma Innovation of the Year' Award from the Government of India. -Glenmark is the first company to launch in India a Triple FDC of Teneligliptin Pioglitazone Metformin for Adults with Type 2 Diabetes & High Insulin Resistance. -Glenmark Pharmaceuticals launches Fingolimod Capsules, 0.5 mg in the US. 2023 -"Glenmark Pharmaceuticals launches Bumetanide Injection USP, 1 mg/4 mL (0.25mg/mL) Single-Dose Vials and 2.5 mg/10 mL (0.25 mg/mL) Multi-Dose Vials". 2024 -Glenmark Pharmaceuticals eceived approval from the US health regulator to market a generic medication to treat conditions caused by too much acid production in the stomach. -Glenmark Pharmaceuticals Inc. USA launches Lacosamide Oral Solution, 10 mg/mL. -Glenmark Pharmaceuticals Inc. USA launches Travoprost Ophthalmic Solution USP, 0.004% . -Glenmark Pharmaceuticals receives ANDA approval for Topiramate Capsules USP, 15 mg and 25 mg -Glenmark and BeiGene Enter into an Agreement for Marketing and Distribution of Tislelizumab and Zanubrutinib in India.

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Parent Organisation

Glenmark Pharmaceuticals Ltd.

Founded

18/11/1977

Managing Director

Mr.Glenn Saldanha

NSE Symbol

GLENMARKEQ

FAQ

The current price of Glenmark Pharmaceuticals Ltd is ₹ 1440.10.

The 52-week high for Glenmark Pharmaceuticals Ltd is ₹ 1464.10 and the 52-week low is ₹ 1427.10.

The market capitalization of Glenmark Pharmaceuticals Ltd is currently ₹ 40639.74. This value can fluctuate based on stock price movements and changes in the number of shares outstanding.

To buy Glenmark Pharmaceuticals Ltd shares, you need to have a brokerage account. First, choose a reputable brokerage firm, open an account, and complete the necessary KYC procedures.

To invest in Glenmark Pharmaceuticals Ltd, you need a brokerage account. After opening an account and completing the KYC process, you can fund your account and use the trading platform to purchase Glenmark Pharmaceuticals Ltd shares.

The CEO of Glenmark Pharmaceuticals Ltd is Mr.Glenn Saldanha, who has been leading the company with a vision to expand its renewable energy portfolio and drive sustainable growth.

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