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Allopurinol

NDC 71921-241 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerFlorida Pharmaceutical Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204467
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (200 mg/1)
Marketing started20250522
Package count1

External sources

Source: openFDA. Public-domain (CC0).