USFDA gives nod to Lupin for this drug to treat Kidney disease

This product will be manufactured at the company's Goa facility

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USFDA
Picture: Pixabay

Last Updated on December 28, 2021 by The Health Master

Drug firm Lupin on Saturday said it has received approval from the US health regulator to market Sevelamer Carbonate for Oral Suspension, used in the control of serum phosphorus with chronic kidney disease (CKD) on dialysis.

The company has received approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) Sevelamer Carbonate for Oral Suspension in the American market, Lupin said in a statement.

This product will be manufactured at the company’s Goa facility, it added.

As per IQVIA MAT September 2021 data, Sevelamer Carbonate for Oral Suspension had an estimated annual sales of $51.7 million in the US.

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