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Docetaxel

NDC 47335-895 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA022534
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDOCETAXEL ANHYDROUS (80 mg/4mL)
Marketing started20201126
Package count1

External sources

Source: openFDA. Public-domain (CC0).