Lupin receives US FDA approval for kidney ailment tabs
17 June 2021 | News
The product will be manufactured at Lupin’s facility in Nagpur
Lupin has received approval for its Sevelamer Hydrochloride Tablets, 400 mg and 800 mg from the US FDA to market a generic equivalent of Renagel tablets, 400 mg and 800 mg, of Genzyme Corporation. The product will be manufactured at Lupin’s facility in Nagpur
Sevelamer hydrochloride tablets are indicated for the control of serum phosphorus in patients with chronic kidney disease (CKD) on dialysis. Sevelamer Hydrochloride Tablets (RLD: Renagel) had estimated annual sales of $80 million in the US.
