NDC 0955-1020 – Docetaxel

Docetaxel 20 mg/mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug 1 recall

Product NDC0955-1020

Product details

Brand name
Docetaxel
Generic name
Docetaxel
Labeler
Sanofi-Aventis U.S. LLC
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
NDA AUTHORIZED GENERIC · NDA020449
Marketed since
October 21, 2010
Listing expires
December 31, 2026
Pharmacologic class
Microtubule Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Docetaxel →

Package NDC codes (1)

Package NDCDescriptionSince
0955-1020-011 VIAL, GLASS in 1 CARTON (0955-1020-01) / 1 mL in 1 VIAL, GLASSOct 21, 2010

Recalls mentioning this NDC

Other Docetaxel products