Lupin stock rises nearly 3% after US FDA approves Allopurinol tablets
Global pharma major Lupin Limited (Lupin) today announced that it has received approval from the United States Food and Drug Administration (U.S. FDA) for its abbreviated new drug application for Allopurinol tablets USP, 100 mg and 300 mg. The drug will be manufactured at Lupin’s Pithampur facility in India.
The medicines will be used for adult patients with signs and symptoms of primary or secondary gout (acute attacks, tophi, joint destruction, uric acid lithiasis, and/or nephropathy), among other treatments.