FDA NDC Directory · JSON-LD · Markdown

Azathioprine

NDC 68462-502 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGlenmark Pharmaceuticals, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA075252
Dosage form / routeTABLET · ORAL
Active ingredientsAZATHIOPRINE (50 mg/1)
Marketing started19990801
Package count1

External sources

Source: openFDA. Public-domain (CC0).