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Allopurinol

NDC 82638-112 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHarman Finochem Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214443
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (100 mg/1)
Marketing started20231006
Package count4

External sources

Source: openFDA. Public-domain (CC0).