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Azathioprine Sodium

NDC 0143-9566 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074419
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsAZATHIOPRINE SODIUM (100 mg/10mL)
Marketing started19950501
Package count1

External sources

Source: openFDA. Public-domain (CC0).