USFDA gives approval for this tablet to treat High BP

This is a generic equivalent of Edarbi® tablets, 40 mg, and 80 mg, of Azurity Pharmaceuticals, Inc.

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USFDA Approval
USFDA Approval

Last Updated on October 15, 2024 by The Health Master

Mumbai: Lupin Limited announced that it has received approval from the United States Food and Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA), Azilsartan Medoxomil tablets, 40 mg, and 80 mg, to market.

This is a generic equivalent of Edarbi® tablets, 40 mg, and 80 mg, of Azurity Pharmaceuticals, Inc.

Azilsartan is used to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems.

The product will be manufactured at Lupin’s facility in Nagpur, India. In 2011, Azilsartan Medoxomil Tablets (RLD Edarbi®) had an estimated annual sales of USD 101 million in the US.

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