Glenmark gets USFDA nod for Milnacipran Hydrochloride tablets

PTI New Delhi | Updated on January 15, 2018 Published on March 31, 2017

Glenmark Pharmaceuticals has received tentative approval from the USFDA for Milnacipran Hydrochloride tablets.

“Glenmark Pharmaceuticals Inc, USA, has been granted tentative approval by the United States Food and Drug Administration (USFDA) for Milnacipran Hydrochloride tablets, 12.5 mg, 25 mg, 50 mg and 100 mg,” the company said in a BSE filing.

Milnacipran Hydrochloride tablets are generic version of Savella drug, 12.5 mg, 25 mg, 50 mg and 100 mg of Allergan Sales LLC.

Citing IMS Health data for the 12 months to February 2017, Glenmark said the Savella tablets achieved annual sales of approximately $154.4 million.

The company’s current portfolio consists of 113 products authorised for distribution in the US marketplace and 65 ANDA pending approval with the USFDA.

Glenmark stock was trading 0.39 per cent down at Rs 860.60 on the BSE.

Published on March 31, 2017
This article is closed for comments.
Please Email the Editor