USFDA gives nod for this generic medication for high BP

The Cozaar tablets produced by Organon LLC and manufactured by the Hyderabad-based company are bioequivalent.

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USFDA Approval
USFDA Approval

Last Updated on October 17, 2024 by The Health Master

Granules India announced on Monday that it has received approval from the US Food and Drug Administration (USFDA) to market a generic product to treat high blood pressure.

According to Granules India, the US Food & Drug Administration (USFDA) has given the company the go-ahead to market Losartan Potassium tablets in strengths of 25 mg, 50 mg, and 100 mg.

The Cozaar tablets produced by Organon LLC and manufactured by the Hyderabad-based company are bioequivalent.

According to IQVIA/IMS Health, the current annual US market for Losartan potassium tablets is around USD 336 million.

On the BSE, the company’s shares were trading 1.24 percent lower at Rs 281.75 per share.

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