Gemcitabine 00409-0183
Product NDC
00409-0183- Manufacturer
- Hospira, Inc.
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- August 24, 2011
- Listing Expires
- December 31, 2027
- Application
- NDA200795
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Gemcitabine Hydrochloride | 38 mg/mL |
Drug Class
Nucleic Acid Synthesis Inhibitors [MoA]Nucleoside Metabolic Inhibitor [EPC]
Packaging Options(1)
1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0183-01) / 5.26 mL in 1 VIAL, SINGLE-DOSE