FDA NDC Directory · JSON-LD · Markdown

ALLOPURINOL

NDC 72189-417 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA204467
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (300 mg/1)
Marketing started20230202
Marketing ended20291031
Package count2

External sources

Source: openFDA. Public-domain (CC0).