Lupin receives USFDA approval for Sevelamer Carbonate Tablets

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Capital Market
Last Updated : Jan 25 2021 | 12:31 PM IST
Lupin has received approval for its Sevelamer Carbonate Tablets, 800 mg, from the United States Food and Drug Administration, to market a generic equivalent of Renvele Tablets, 800 mg, of Genzyme Corporation.

Sevelamer Carbonate Tablets, 800 mg, are indicated for the control of serum phosphorus in adults and children 6 years of age and older with chronic kidney disease on dialysis.

Sevelamer Carbonate Tablets (RLD: Renvele) had estimated annual sales of USD 348 million in the U.S. (IQVIA MAT September 2020).

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First Published: Jan 25 2021 | 12:20 PM IST

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