Glenmark gets tentative nod from USFDA for epilepsy drug
Glenmark Pharmaceuticals shares were trading at Rs 787.20 in the morning deals on the BSE, down 2.95%18-03-2016
Glenmark gets tentative nod from USFDA for epilepsy drug
Glenmark Pharmaceuticals shares were trading at Rs 787.20 in the morning deals on the BSE, down 2.95%Glenmark Pharmaceuticals receives tentative ANDA approval for Lacosamide Oral Solution, 10 mg/mL
Glenmark Pharmaceuticals Ltd has informed BSE regarding a Press Release dated March 18, 2016 titled "Glenmark Pharmaceuticals receives tentative ANDA approval for Lacosamide Oral Solution, 10 mg/mL".Govt bans Crocin Cold and Flu, D-Cold Total
Top five companies which are going to take the hit are - Abbott, Pfizer, Macleods, Glenmark and MankindTemporary relief to Abbott, Glenmark in drug case
The government banned 344 drug combinations over the weekend, including Abbott's codeine-based cough syrup, after a government panel of experts found they had "no therapeutic justification."Glenmark gets final FDA nod for migraine headache relief drug
The company's current portfolio consists of 61 ANDAs pending approvals from the US FDAGlenmark Pharmaceuticals receives ANDA approval for Frovatriptan Succinate Tablets, 2.5 mg
Glenmark Pharmaceuticals Ltd has informed BSE regarding a Press Release dated March 14, 2016 titled "Glenmark Pharmaceuticals receives ANDA approval for Frovatriptan Succinate Tablets, 2.5 mg".Glenmark Gets USFDA Nod for Contraceptive Tablets
According to IMS Health sales data for the 12 months to December 2015, the Ortho Tri-cyclen Lo tablets achieved annual sales of around $503.9 million, Glenmark said.Glenmark Pharmaceuticals receives ANDA approval for Norgestimate and Ethinyl Estradiol Tablets USP, 0.18 mg/0.025 mg, 0.215 mg/0.025 mg, and 0.25 mg/0.025 mg
Glenmark Pharmaceuticals Ltd has informed BSE regarding a Press Release dated February 24, 2016, titled "Glenmark Pharmaceuticals receives ANDA approval for Norgestimate and Ethinyl Estradiol Tablets USP, 0.18 mg/0.025 mg, 0.215 mg/0.025 mg, and 0.25 mg/0.025 mg".Glenmark gets tentative nod from USFDA for azelaic acid gel
The patent for Finacea topical gel, 15%, is scheduled to expire on November 18, 2018Glenmark Pharmaceuticals receives tentative ANDA approval for Azelaic Acid Gel, 15%
Glenmark Pharmaceuticals Ltd has informed BSE regarding a Press Release dated February 17, 2016, titled "Glenmark Pharmaceuticals receives tentative ANDA approval for Azelaic Acid Gel, 15%".