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Glenmark gets USFDA nod for leukemia treatment drug

The company's shares were trading up over 1% on the BSE.

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Glenmark Pharmaceuticals has received final approval from the US health regulator USFDA for sale of Tretinoin Capsules, used in treatment of leukemia.

"Glenmark Pharmaceuticals Inc., USA has been granted final approval by the United States Food & Drug Administration (U.S.
FDA) for Tretinoin Capsules, 10 mg," the company said in a BSE filing.

The approved product is generic version of Vesanoid Capsules, 10 mg, of Hoffmann La Roche, Inc. (which is no longer being marketed in the US), the company added.

According to IMS Health sales data for the 12 months to October 2016, Glenmark said the Vesanoid Capsules, 10 mg market achieved annual sales of approximately $22.0 million.

The company's current portfolio consists of 112 products authorised for distribution in the US marketplace and 63 ANDA pending approval with the USFDA.

Shares of Glenmark Pharmaceuticals were trading 1.09% up, at Rs 898.75 in the morning trade on BSE.

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