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Allopurinol

NDC 53489-157 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071450
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (300 mg/1)
Marketing started19870109
Package count5

External sources

Source: openFDA. Public-domain (CC0).