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Docetaxel

NDC 67457-781 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerMylan Institutional LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208137
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsDOCETAXEL (20 mg/mL)
Marketing started20190618
Package count1

External sources

Source: openFDA. Public-domain (CC0).