Oxaliplatin 00781-3317
Product NDC
00781-3317- Manufacturer
- Sandoz Inc
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA078817
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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, SINGLE-USE in 1 CARTON (0781-3317-80) / 20 mL in 1 VIAL, SINGLE-USE