Docetaxel 47335-0895-40

Package NDC

47335-0895-40

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: November 26, 2020
Listing Expires: December 31, 2026
Application: NDA022534

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Active Ingredients

Ingredient	Strength
Docetaxel Anhydrous	80 mg/4mL

Drug Class

Microtubule Inhibitor [EPC]Microtubule Inhibition [PE]Microtubule Inhibitor [EPC]

Selected Package

47335-0895-40Selected

1 VIAL, GLASS in 1 CARTON (47335-895-40) / 4 mL in 1 VIAL, GLASS