NDC 68001-342 – Gemcitabine

Gemcitabine Hydrochloride 100 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC68001-342

Product details

Brand name
Gemcitabine
Generic name
Gemcitabine
Labeler
BluePoint Laboratories
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA209604
Marketed since
May 25, 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
68001-342-341 VIAL, MULTI-DOSE in 1 CARTON (68001-342-34) / 2 mL in 1 VIAL, MULTI-DOSEMay 25, 2018

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