Gemcitabine 00143-9342-01

Package NDC

00143-9342-01

Manufacturer: Hikma Pharmaceuticals Usa Inc.
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: October 17, 2025
Listing Expires: December 31, 2026
Application: ANDA213175

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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

00143-9342-01Selected

1 VIAL in 1 CARTON (0143-9342-01) / 52.6 mL in 1 VIAL