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Allopurinol

NDC 0904-6572 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameallopurinol
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA075798
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (300 mg/1)
Marketing started20030627
Package count1

External sources

Source: openFDA. Public-domain (CC0).