Gemcitabine 68001-0359-37

Package NDC

68001-0359-37

Manufacturer: Bluepoint Laboratories
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: May 25, 2018
Listing Expires: December 31, 2026
Application: NDA209604

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Active Ingredients

Ingredient	Strength
Gemcitabine Hydrochloride	100 mg/mL

Drug Class

Nucleic Acid Synthesis Inhibitors [MoA]Nucleoside Metabolic Inhibitor [EPC]

Selected Package

68001-0359-37Selected

1 VIAL, MULTI-DOSE in 1 CARTON (68001-359-37) / 20 mL in 1 VIAL, MULTI-DOSE