Cisplatin 68001-0609
Product NDC
68001-0609- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA207323
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cisplatin | 1 mg/mL |
Drug Class
Platinum-based Drug [EPC]Platinum-based Drug [EPC]Platinum-containing Compounds [EXT]
Packaging Options(1)
1 VIAL in 1 CARTON (68001-609-33) / 100 mL in 1 VIAL