Gemcitabine 71288-0114-50

Generic: Gemcitabine Hydrochloride

Package NDC

71288-0114-50

Manufacturer: Meitheal Pharmaceuticals Inc.
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: November 1, 2018
Listing Expires: December 31, 2026
Application: ANDA091365

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Active Ingredients

Ingredient	Strength
Gemcitabine Hydrochloride	1 g/1

Drug Class

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

Selected Package

71288-0114-50Selected

1 VIAL, SINGLE-DOSE in 1 CARTON (71288-114-50) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE