Lupin gets USFDA nod for generic drug


Drug maker Lupin on September 9 said it has received approval from the US health regulator to market Ethacrynic Acid tablets, used to treat edema in various conditions, in the American market.

The company has received approval from the US Food and Drug Administration (USFDA) to market its product, a generic version of Bausch Health’s Edecrin tablets, in 25 mg strength, Lupin said in a statement.

As per IQVIA MAT June 2019 data, Ethacrynic Acid tablets had annual sales of around USD 24 million (about Rs 170 crore) in the US.
Shares of Lupin on September 9 ended 0.82 percent lower at Rs 766.20 apiece on the BSE.

News Source: Moneycontrol

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