Lupin Receives Approval for Sevelamer Carbonate Tablets

Monday January 25, 2021 at 12:38 pm

Mumbai, Baltimore, January 25, 2021: Lupin Limited (Lupin), global pharmaceutical company, announced today that it has received approval for its Sevelamer Carbonate Tablets, 800 mg, from the United States Food and Drug Administration, to market a generic equivalent of Renvela® 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: Renvela®) had estimated annual sales of USD 348 million in the U.S. (IQVIA MAT September 2020).

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