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Allopurinol

NDC 55111-730 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameallopurinol
Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA071587
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (300 mg/1)
Marketing started20091001
Package count2

External sources

Source: openFDA. Public-domain (CC0).