Gemcitabine 16714-0909-01

Generic: Gemcitabine Hydrochloride

Package NDC

16714-0909-01

Manufacturer: Northstar Rx Llc
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	200 mg/1

Drug Class

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

Selected Package

16714-0909-01Selected

1 VIAL, SINGLE-DOSE in 1 CARTON (16714-909-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE