FDA NDC Directory · JSON-LD · Markdown

Allopurinol

NDC 70518-4556 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204467
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (300 mg/1)
Marketing started20260126
Package count1

External sources

Source: openFDA. Public-domain (CC0).