USFDA gives nod to Lupin for Sevelamer Hydrochloride Tablets, 800 mg

Sevelamer Hydrochloride Tablets, 800 mg is a generic equivalent of Renagel® Tablets, 800 mg of Genzyme Corporation.

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USFDA Approval
USFDA Approval

Last Updated on October 15, 2024 by The Health Master

Mumbai: Lupin Limited announced the launch of Sevelamer Hydrochloride Tablets, 800 mg, having received approval from the United States Food and Drug Administration (USFDA). The product will be manufactured at Lupin’s facility in Nagpur, India.

Sevelamer Hydrochloride Tablets, 800 mg is a generic equivalent of Renagel® Tablets, 800 mg of Genzyme Corporation.

Sevelamer Hydrochloride Tablets, 800 mg (RLD: Renagel) had estimated annual sales of $75 million in the US (IQVIA MAT December 2021).

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