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Busulfan

NDC 67457-893 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerMylan Institutional LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208536
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsBUSULFAN (6 mg/mL)
Marketing started20171121
Marketing ended20260531
Package count1

External sources

Source: openFDA. Public-domain (CC0).