Investors Financial Results

Announcements 2023

Intimation of Schedule of Analyst / Institutional Investor Meetings November 2023

Glenmark’s Q2 FY 2023-24 Results – Newspaper Advertisement

Glenmark’s Q2 FY 2023-24 Results

Glenmark’s MDA Q2 FY 2023 – 24

Glenmark Pharma reports consolidated revenue growth of 6.3% and adjusted EBITDA growth of 8.3% YoY for Q2 FY 2023-24

Result of Postal Ballot by remote e-voting & Scrutinizer's Report

Glenmark Pharmaceuticals receives ANDA approval for Fluphenazine Hydrochloride Tablets USP, 1 mg, 2.5 mg, 5 mg, and 10 mg

Q2 FY24 Earnings Call Invitation – November 15, 2023

Board Meeting intimation – 10 November 2023

Glenmark Pharma is first to launch a Triple-drug FDC of Teneligliptin + Dapagliflozin + Metformin in India for Type 2 Diabetes in Adults with Co-morbidities

Glenmark Pharmaceuticals receives ANDA approval for Apremilast Tablets, 10 mg, 20 mg and 30 mg

Ichnos Sciences Enters Licensing Agreement For OX40 Antagonist Monoclonal Antibody Portfolio with Astria Therapeutics OCT 23

Newspaper Advertisement – Postal Ballot Notice

Notice of Postal Ballot - Disclosure under Regulation 30 of the SEBI LODR Regulations, 2015

Board Meeting Outcome for Outcome Of The Board Meeting Held On October 05, 2023

Credit Ratings -rating rationale issued by India Ratings and Research.

Proceedings and Scrutinizer’s Report

Chairman's Speech at the 45th AGM

Credit Rating -CRISIL Rating Rationale

Credit Rating- Glenmark Pharmaceuticals Outlook Revised to Positive on proposed GLS Stake Sale; ''BB'' Rating Affirmed

Cosmo and Glenmark announce the signing of Distribution and License Agreements for Winlevi® in Europe and South Africa

Credit Rating-India Ratings has discontinued and withdrawn the outstanding voluntary issuer ratings disclosure due to regulatory requirements.

Intimation of Analyst-Investor Meet, September 2023

Glenmark Pharma announces Proposed Divestment of Majority Stake in Glenmark Life Sciences

Board Meeting Outcome for Outcome Of The Board Meeting Held On September 21, 2023

Change in Senior Management September 2023

45th AGM Notice - Newspaper Advertisement

Glenmark AGM Notice 2023

Intimation of 45th Annual General Meeting

Press Release of our wholly owned subsidiary company relating to Antitrust settlement with DOJ

Glenmark Pharmaceuticals receives sANDA approval for Tacrolimus Ointment, 0.03%

Change in Senior Management August 2023

Regulation 30 (LODR)-Change in Directorate

Glenmark’s MDA Q1 FY 2023 – 24

Glenmark’s Q1 FY 2023-24 Results

Glenmark Pharma reports revenue growth of 22.5%, EBITDA growth of 46.2% YoY for Q1 FY 2023-24

Result of Postal Ballot by remote e-voting & Scrutinizer's Report

Q1 FY24 Earnings Call Invitation – August 14, 2023

Glenmark Pharmaceuticals receives ANDA approval for Saxagliptin Tablets, 2.5 mg and 5 mg

Board Meeting intimation – 31st July, 2023

Regulation 30 (LODR)-Updates on Acquisition

Newspaper Advertisement for transfer of equity shares to IEPF Authority

Newspaper Advertisement - Regulation 47 of SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015

Notice of Postal Ballot - Disclosure under Regulation 30 of the SEBI LODR Regulations, 2015

Update On The Company''s Monroe, North Carolina (USA) Facility

Exchange Notification: Glenmark becomes a part of the Science Based Targets initiative, sets GHG emissions targets for FY 2035

Outcome of the Board Meeting

Disclosure Of Related Party Transactions For The Half Year Ended 31st March, 2023

Glenmark Pharma reports revenue growth of 11.7% YoY Q4; 5.6% for the full year FY 2022-23

Glenmark’s Q4 FY 2022-23 Results

Glenmark’s MDA Q4 FY 2022 – 23

Incorporation of a wholly owned subsidiary company

Q4 FY23 Earnings Call Invitation – May 22, 2023

Board Meeting Intimation – 19th May, 2023

Result of Postal Ballot by remote e-voting & Scrutinizer's Report

Glenmark Pharmaceuticals receives ANDA approval for Calcipotriene and Betamethasone Dipropionate Foam, 0.005%|0.064%

Glenmark Pharmaceuticals receives ANDA approval for Prochlorperazine Maleate Tablets USP, 5 mg and 10 mg

Glenmark receives acceptance from U.S. FDA on its IND application for GRC 54276 to proceed with a Phase 1/2, first-in-human clinical study of the molecule for the treatment of patients with advanced solid tumors and lymphomas

Newspaper Advertisement - Postal Ballot Notice

Notice of Postal Ballot - Disclosure under Regulation 30 of the SEBI LODR Regulations, 2015

Glenmark Pharmaceuticals receives ANDA approval for Clindamycin Hydrochloride Capsules USP, 75 mg, 150 mg, and 300 mg

Glenmark and Cediprof Announce Exclusive Distribution Agreement in the United States for U.S. FDA Approved Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and
Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product), 5 mg, 10 mg, 15 mg,
20 mg and 30 mg

Glenmark Pharmaceuticals receives 2nd ANDA tentative approval for Saxagliptin Tablets, 2.5 mg and 5 mg

Newspaper Publication of Q3 FY 2022-23 Result

Glenmark’s Q3 FY 2022-23 Results

Glenmark's MDA Q3 FY 2022 – 23

Glenmark Pharma reports revenue growth of 9.2% and PAT growth of 21.3% YoY for Q3 FY 2022-23

Glenmark launches AKYNZEO® I.V. in India – First Fixed I.V. Antiemetic Combination for the Prevention of Chemotherapy-induced Nausea and Vomiting

Q3 FY23 Earnings Call Invitation – February 13, 2023

Heart failure treatment becomes more affordable with Glenmark launching the Sacubitril + Valsartan tablets in India

Glenmark Pharmaceuticals launches Bumetanide Injection USP, 1 mg/4 mL (0.25 mg/mL) Single-Dose Vials and 2.5 mg/10 mL (0.25 mg/mL) Multi-Dose Vials

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