NDC 0409-0187 – Gemcitabine

Gemcitabine Hydrochloride 38 mg/mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC0409-0187

Product details

Brand name
Gemcitabine
Generic name
Gemcitabine
Labeler
Hospira, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA079183
Marketed since
November 15, 2010
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
0409-0187-011 VIAL, SINGLE-DOSE in 1 CARTON (0409-0187-01) / 50 mL in 1 VIAL, SINGLE-DOSENov 15, 2010

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