Oxaliplatin 00955-1731
Product NDC
00955-1731- Manufacturer
- Winthrop U.s, A Business Of Sanofi-Aventis U.s. Llc
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- September 1, 2015
- Listing Expires
- December 31, 2026
- Application
- NDA021759
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxaliplatin | 5 mg/mL |
Drug Class
Platinum-based Drug [EPC]Platinum-based Drug [EPC]Platinum-containing Compounds [EXT]
Packaging Options(1)
1 VIAL, GLASS in 1 CARTON (0955-1731-10) / 10 mL in 1 VIAL, GLASS