NDC 63323-102 – Gemcitabine

Gemcitabine Hydrochloride 200 mg/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC63323-102

Product details

Brand name
Gemcitabine
Generic name
Gemcitabine
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA090799
Marketed since
July 26, 2011
Listing expires
December 31, 2026
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Gemcitabine →

Package NDC codes (2)

Package NDCDescriptionSince
63323-102-131 VIAL, SINGLE-DOSE in 1 BOX (63323-102-13) / 5 mL in 1 VIAL, SINGLE-DOSEJul 26, 2011
63323-102-941 VIAL, SINGLE-DOSE in 1 BOX (63323-102-94) / 5 mL in 1 VIAL, SINGLE-DOSEJul 26, 2011

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