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Lupin Gets USFDA Nod To Market Generic Diabetes Drug

The company's product is a generic equivalent of AstraZeneca AB's Qtern tablets, it added.

<div class="paragraphs"><p>Lupin's manufacturing facility in Goa. (Source: Company website)</p></div>
Lupin's manufacturing facility in Goa. (Source: Company website)

Drug firm Lupin on Thursday said it has received approval from the U.S. health regulator to market a generic medication to treat diabetes.

The company has received approval from the U.S. Food and Drug Administration (USFDA) for its abbreviated new drug application for Dapagliflozin and Saxagliptin tablets, the Mumbai-based drug maker said in a regulatory filing.

The company's product is a generic equivalent of AstraZeneca AB's Qtern tablets, it added.

This generic product will be manufactured at its Pithampur facility, the company said.

Dapagliflozin and Saxagliptin tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

As per IQVIA data, Dapagliflozin and Saxagliptin tablets had estimated annual sales of $5 million in the U.S. market.