NDC 25021-239 – Gemcitabine

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

Human Prescription Drug

Product NDC25021-239

Product details

Brand name
Gemcitabine
Generic name
Gemcitabine
Labeler
Sagent Pharmaceuticals
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA209077
Marketed since
January 15, 2019
Listing expires
December 31, 2026
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Gemcitabine →

Package NDC codes (3)

Package NDCDescriptionSince
25021-239-051 VIAL in 1 CARTON (25021-239-05) / 5.26 mL in 1 VIALJan 15, 2019
25021-239-261 VIAL in 1 CARTON (25021-239-26) / 26.3 mL in 1 VIALJan 15, 2019
25021-239-521 VIAL in 1 CARTON (25021-239-52) / 52.6 mL in 1 VIALJan 15, 2019

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