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Docetaxel

NDC 57884-3043 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerJiangsu Hengrui Pharmaceuticals Co., Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA207252
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsDOCETAXEL (160 mg/8mL)
Marketing started20170809
Package count1

External sources

Source: openFDA. Public-domain (CC0).