NDC 0955-1022 – Docetaxel

Docetaxel 160 mg/8mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug 1 recall

Product NDC0955-1022

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 23, 2016
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
0955-1022-081 VIAL, GLASS in 1 CARTON (0955-1022-08) / 8 mL in 1 VIAL, GLASSOct 23, 2016

Recalls mentioning this NDC

Other Docetaxel products