NDC 0143-9342 – Gemcitabine

Gemcitabine Hydrochloride 38 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0143-9342

Product details

Brand name
Gemcitabine
Generic name
Gemcitabine
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA213175
Marketed since
October 17, 2025
Listing expires
December 31, 2026
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Gemcitabine →

Package NDC codes (1)

Package NDCDescriptionSince
0143-9342-011 VIAL in 1 CARTON (0143-9342-01) / 52.6 mL in 1 VIALOct 17, 2025

Recalls mentioning this NDC

Other Gemcitabine products