Newsroom

Newsroom - 2017

Glenmark receives ANDA approval for Norethindrone Acetate and Ethinyl Estradiol Tablets USP and Ferrous Fumarate Tablets, 1 mg/20 mcg

Glenmark Announces Top-Line Results from a Phase 3 Safety Study Evaluating Ryaltris™ in Patients with Perennial Allergic Rhinitis

Glenmark Pharmaceuticals Announces Dosing of First Patient With Investigational Immuno-Oncology Agent GBR 1342

Glenmark announces successful closure of the decentralised registration procedure (DCP) for generic Seretide® Accuhaler® in the Nordic region

Glenmark Pharmaceuticals receives ANDA approval for HAILEY TM Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets USP, 1 mg/20 mcg and Ferrous Fumarate Tablets)

Glenmark Pharmaceuticals receives ANDA approval for HAILEY 24 Fe (Norethindrone Acetate and Ethinyl Estradiol Tablets, USP and Ferrous Fumarate Tablets), 1 mg/20 mcg

Glenmarks consolidated revenue increases by 1.46 percent to Rs. 22,565.90 Mn. for Q2 FY 2017 – 18

Glenmark presents New Data from Respiratory Portfolio at the ACAAI Annual Scientific Meeting 2017

Glenmark receives ANDA approval for Aprepitant Capsules USP

Glenmark receives ANDA approval for Desonide Lotion

Glenmark receives ANDA approval for Nitroglycerin Sublingual Tablets USP, 0.3 mg, 0.4 mg, and 0.6 mg

Glenmark receives ANDA approval for Desonide Ointment

Glenmark receives ANDA approval for Propafenone Hydrochloride Extended-Release Capsules

Glenmark receives ANDA approval for Triamcinolone Acetonide Ointment USP, 0.1%

Glenmark Pharmaceuticals receives ANDA approval for Acyclovir Ointment USP, 5%

Glenmark Pharmaceuticals Reports Positive Data in a Phase 2a Study of GBR 830 for the Treatment of Patients with Atopic Dermatitis

Glenmark’s consolidated revenue increases by 19.99% to Rs. 23,630.02 Mn for Q1 FY 2017 – 18

Glenmark receives ANDA approval for Desonide Cream, 0.05%

Glenmark Pharmaceuticals Enters Exclusive Agreement with Cyndea Pharma S.L. for Generic Soft-Gelatin Capsule Drug Products

Glenmark receives ANDA approval for Amlodipine and Olmesartan Medoxomil Tablets

Glenmark Pharmaceuticals receives MHRA Approval for Maloff Protect as Pharmacy license in the UK

Glenmark receives ANDA approval for Indomethacin Extended-Release Capsules USP-75mg

Glenmark Pharmaceuticals Receives Tentative ANDA Approval For Solifenacin Succinate Tablets, 5 mg and 10 mg

Glenmark Pharmaceuticals Licenses Small Molecule Oncology Compound from APC Therapeutics to Expand Immuno-Oncology Portfolio

Tentative ANDA approval for Saxagliptin Tablets, 2.5 mg and 5 mg

ANDA approval for Atomoxetine Capsules USP, 10 mg, 18 mg, 25 mg, 40 mg, 60 mg, 80 mg and 100 mg

ANDA approval for Nebivolol Tablets, 2.5 mg, 5 mg, 10 mg and 20 mg

ANDA approval for Olmesartan Medoxomil Tablets, 5 mg, 20 mg and 40 mg

Glenmark Pharmaceuticals to Initiate Clinical Study for GBR 1342

Glenmark's consolidated revenue increased by 6.52% to Rs. 24,571.83 Mn for Q4 FY 2016 -- 17

Glenmark Pharmaceuticals Initiates Clinical Investigation for GBR 310, its Proposed Biosimilar Candidate for XOLAIR®

Glenmark Pharmaceuticals receives tentative ANDA approval for Dabigatran Etexilate Capsules, 75 mg, 110 mg and 150 mg

Glenmark Pharmaceuticals receives ANDA approval for Fenofibrate Capsules USP, 67 mg, 134 mg and 200 mg

Glenmark Pharmaceuticals receives tentative ANDA approval for Milnacipran Hydrochloride Tablets, 12.5 mg, 25 mg, 50 mg and 100 mg

Glenmark Pharmaceuticals reports positive results from a Phase 3 trial of GSP 301

Glenmark Pharmaceuticals receives tentative ANDA approval for Fingolimod Capsules, 0.5 Mg

Glenmark Pharmaceuticals Receives FDA Clearance of IND for GSP 304

Glenmark Pharmaceuticals and Evestra, Inc. Announce Partnership Agreement for Generic NuvaRing®

Glenmark’s consolidated revenue increases by 42.55 % to Rs. 25,350.08 Mn for Q3 FY 2016 – 17

Glenmark Pharmaceuticals Receives FDA Clearance of IND for GBR 1302-BEAT™ Phase I Trial