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Allopurinol

NDC 0591-5544 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA018877
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (300 mg/1)
Marketing started20090406
Marketing ended20270430
Package count2

External sources

Source: openFDA. Public-domain (CC0).