Gemcitabine 68001-0359
Product NDC
68001-0359- 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]
Packaging Options(1)
1 VIAL, MULTI-DOSE in 1 CARTON (68001-359-37) / 20 mL in 1 VIAL, MULTI-DOSE