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Azathioprine

NDC 65841-602 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077621
Dosage form / routeTABLET · ORAL
Active ingredientsAZATHIOPRINE (50 mg/1)
Marketing started20070711
Package count2

External sources

Source: openFDA. Public-domain (CC0).