Allopurinol 71921-0241-09

Package NDC

71921-0241-09

Product NDC: 71921-0241

Manufacturer: Florida Pharmaceutical Products, Llc
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 22, 2025
Listing Expires: December 31, 2027
Application: ANDA204467

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Active Ingredients

Ingredient	Strength
Allopurinol	200 mg/1

Drug Class

Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitors [MoA]

Selected Package

71921-0241-09Selected

90 TABLET in 1 BOTTLE (71921-241-09)