FDA NDC Directory · JSON-LD · Markdown

Allopurinol

NDC 69315-409 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214443
Dosage form / routeTABLET · ORAL
Active ingredientsALLOPURINOL (200 mg/1)
Marketing started20240901
Package count1

External sources

Source: openFDA. Public-domain (CC0).