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Doxorubicin Hydrochloride

NDC 0143-9084 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA062975
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDOXORUBICIN HYDROCHLORIDE (2 mg/mL)
Marketing started19960501
Package count1

External sources

Source: openFDA. Public-domain (CC0).