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doxorubicin hydrochloride

NDC 25021-207 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSagent Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA209825
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDOXORUBICIN HYDROCHLORIDE (2 mg/mL)
Marketing started20131031
Package count2

External sources

Source: openFDA. Public-domain (CC0).