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Lupin Gets US Health Regulator Nod for Generic Potassium Deficiency Drug

Lupin gets USFDA nod for generic potassium deficiency drug 



An employee holds tablets inside a coating unit at the Lupin Ltd. pharmaceutical plant (Photographer: Dhiraj Singh/Bloomberg)
An employee holds tablets inside a coating unit at the Lupin Ltd. pharmaceutical plant (Photographer: Dhiraj Singh/Bloomberg)

Drug firm Lupin said its subsidiary Gavis Pharmaceuticals has received final approval from the US health regulator to market potassium chloride extended release capsules, used for treating potassium deficiency in the bloodstream, in the American market. U.S.-based Gavis has received final approval from U.S. Food and Drug Administration (U.S. FDA) to market a generic equivalent of Actavis Labs FL Inc’s potassium chloride extended release capsules in various strengths, Lupin Ltd. said in a regulatory filing.

Lupin had announced acquisition of Somerset-based Gavis Pharmaceuticals on July 23 last year. According to IMS MAT June sales data, potassium chloride extended-release capsules had U.S. sales of $75.4 million.

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