NDC 0409-0183 – Gemcitabine

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

Human Prescription Drug

Product NDC0409-0183

Product details

Brand name
Gemcitabine
Generic name
Gemcitabine
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA200795
Marketed since
July 9, 2013
Listing expires
December 31, 2027
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Gemcitabine →

Package NDC codes (2)

Package NDCDescriptionSince
0409-0183-011 VIAL, SINGLE-DOSE in 1 CARTON (0409-0183-01) / 5.26 mL in 1 VIAL, SINGLE-DOSEAug 24, 2011
0409-0183-251 VIAL, SINGLE-DOSE in 1 CARTON (0409-0183-25) / 5.26 mL in 1 VIAL, SINGLE-DOSEJul 9, 2013

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