NDC 16714-909 – Gemcitabine

Gemcitabine Hydrochloride 200 mg/1 · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC16714-909

Product details

Brand name
Gemcitabine
Generic name
Gemcitabine Hydrochloride
Labeler
NorthStar Rx LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA091365
Marketed since
November 1, 2018
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
16714-909-011 VIAL, SINGLE-DOSE in 1 CARTON (16714-909-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSENov 1, 2018

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