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Docetaxel

NDC 46708-678 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA215744
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsDOCETAXEL ANHYDROUS (10 mg/mL)
Marketing started20230228
Package count3

External sources

Source: openFDA. Public-domain (CC0).