Glenmark gets tentative USFDA nod for generic anti-diabetes tab

The approval granted by the USFDA to Glenmark Pharmaceuticals Inc., USA, is for the strength of 10 mg/5 mg tablets

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USFDA Drug product Approval
USFDA Approval

Last Updated on December 31, 2023 by The Health Master

Glenmark Pharmaceuticals on Wednesday said it has received tentative approval from the US health regulator for its generic Dapagliflozin and Saxagliptin anti-diabetes tablets.

Glenmark Pharma gets tentative USFDA nod for generic anti-diabetes tablets

The approval granted by the United States Food and Drug Administration (USFDA) to Glenmark Pharmaceuticals Inc., USA, is for the strength of 10 mg/5 mg tablets, the generic version of Qtern tablets of the same strength of AstraZeneca AB, the company said in a statement.

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Citing IQVIA sales data for the 12-month period ending February 2020, the company said Qtern tablets, 10 mg/5 mg had achieved annual sales of approximately USD 10.4 million. Glenmark’s current portfolio consists of 162 products authorised for distribution in the US and 44 abbreviated new drug applications pending approval with the USFDA, the company said.