Glenmark Pharmaceuticals has received final approval from the US health regulator for Solifenacin Succinate tablets, used for treatment of overactive bladder.
Glenmark Pharmaceuticals Inc., USA, has been granted final approval by the United States Food and Drug Administration (USFDA) for Solifenacin Succinate tablets in the strengths of 5 mg and 10 mg," the company said in a BSE filing.
Quoting IQVIA sales data for the 12 month period ending March 2019, Glenmark Pharma said the Vesicare tablets, 5 mg and 10 mg market achieved annual sales of approximately USD 942.7 million.
The company's current portfolio consists of 154 products authorised for distribution at the US marketplace and 58 abbreviated new drug applications (ANDAs) pending approval with the USFDA.
Shares of Glenmark Pharma were trading 0.39 per cent higher at Rs 577.91 apiece on BSE.
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