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Doxorubicin Hydrochloride

NDC 70121-1219 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208888
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsDOXORUBICIN HYDROCHLORIDE (2 mg/mL)
Marketing started20170217
Package count1

External sources

Source: openFDA. Public-domain (CC0).