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Azathioprine

NDC 70771-1141 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077621
Dosage form / routeTABLET · ORAL
Active ingredientsAZATHIOPRINE (100 mg/1)
Marketing started20171202
Package count2

External sources

Source: openFDA. Public-domain (CC0).