Gemcitabine 00409-0185-01

Package NDC

00409-0185-01

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: July 26, 2011
Listing Expires: December 31, 2026
Application: ANDA078339

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Active Ingredients

Ingredient	Strength
Gemcitabine Hydrochloride	38 mg/mL

Drug Class

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

Selected Package

00409-0185-01Selected

1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0185-01) / 5 mL in 1 VIAL, SINGLE-DOSE