NDCFind

Docetaxel 00955-1021-04

Package NDC

00955-1021-04

Product NDC: 00955-1021

Manufacturer
Sanofi-Aventis U.s. Llc
Dosage Form
Injection, Solution, Concentrate
Route
Intravenous
Product Type
Human Prescription Drug
Marketing Start
October 21, 2010
Listing Expires
December 31, 2026
Application
NDA020449
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Active Ingredients

IngredientStrength
Docetaxel80 mg/4mL

Drug Class

Microtubule Inhibition [PE]Microtubule Inhibitor [EPC]

Selected Package

00955-1021-04Selected

1 VIAL, GLASS in 1 CARTON (0955-1021-04) / 4 mL in 1 VIAL, GLASS