NDC 25021-254 – Docetaxel

Docetaxel Anhydrous 10 mg/mL · Injection · Intravenous

Human Prescription Drug 2 recalls

Product NDC25021-254

Product details

Brand name
Docetaxel
Generic name
Docetaxel Anhydrous
Labeler
Sagent Pharmaceuticals
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA213510
Marketed since
August 1, 2023
Listing expires
December 31, 2026
Pharmacologic class
Microtubule Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Docetaxel →

Package NDC codes (2)

Package NDCDescriptionSince
25021-254-081 VIAL in 1 CARTON (25021-254-08) / 8 mL in 1 VIALAug 1, 2023
25021-254-161 VIAL in 1 CARTON (25021-254-16) / 16 mL in 1 VIALAug 1, 2023

Recalls mentioning this NDC

Other Docetaxel products