FDA NDC Directory · JSON-LD · Markdown

Allopurinol

NDC 70771-1127 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210117
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (300 mg/1)
Marketing started20180208
Package count3

External sources

Source: openFDA. Public-domain (CC0).