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Allopurinol

NDC 71205-049 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameALLOPURINOL
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203154
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (300 mg/1)
Marketing started20150429
Package count3

External sources

Source: openFDA. Public-domain (CC0).