Glenmark Pharma gets ANDA nod for Esomeprazole Magnesium delayed-Release Capsules

Mumbai, :  Pharma Major, Glenmark Pharmaceuticals Inc., USA (Glenmark) has been granted final approval by the United States Food & Drug Administration (U.S. FDA) for Esomeprazole Magnesium
Delayed-Release Capsules USP, 20 mg and 40 mg, a generic version of Nexium Delayed-Release Capsules, 20 mg and 40 mg, of AstraZeneca Pharmaceuticals LP.
According to IQVIATM sales data for the 12 month period ending March 2019, the Nexium Delayed – Release Capsules, 20 mg and 40 mg market2 achieved annual sales of approximately USD395.1 million, company
said in a filing with BSE.
Glenmark’s current portfolio consists of 153 products authorized for distribution in the U.S. marketplace and 58 ANDA’s pending approval with the U.S. FDA. In addition to these internal filings, Glenmark continues to identify and explore external development partnerships to supplement and accelerate the growth of its existing pipeline and portfolio.
(UNI)