HomeNewsBusinessStocksGlenmark Pharma rises 2% on tentative USFDA nod for Solifenacin Succinate tablets

Glenmark Pharma rises 2% on tentative USFDA nod for Solifenacin Succinate tablets

The company's current portfolio consists of 117 products authorized for distribution in the US market place and 68 ANDA’s pending approval with the USFDA.

June 22, 2017 / 09:30 IST
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Myth 3: Everyone who has a mental illness needs medication to manage symptoms | Bulthuis says no two patients are the same. While medicines can help manage symptoms, there are some people with mental illness who do not require medication. For others, medicine is essential for recovery. (Representative image)
Myth 3: Everyone who has a mental illness needs medication to manage symptoms | Bulthuis says no two patients are the same. While medicines can help manage symptoms, there are some people with mental illness who do not require medication. For others, medicine is essential for recovery. (Representative image)

Moneycontrol News

Shares of pharma major Glenmark Pharma rose as much as 2.5 percent intraday Thursday as it has received tentative USFDA nod for Solifenacin Succinate tablets.

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"Glenmark Pharmaceuticals Inc., USA has been granted tentative approval by the United States Food & Drug Administration (USFDA) for Solifenacin Succinate tablets, 5 mg and 10 mg, which is a generic version of Vesicare tablets, 5 mg and 10 mg of Astellas Pharma US Inc," as per company release.

The Vesicare tablets achieved annual sales of approximately USD 1.1 billion for the 12 month period ending April 2017, as per IMS Health sales data.