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Allopurinol

NDC 50090-4662 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA211820
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (100 mg/1)
Marketing started20190312
Package count2

External sources

Source: openFDA. Public-domain (CC0).