Docetaxel 57884-3041
Product NDC
57884-3041- Manufacturer
- Jiangsu Hengrui Pharmaceuticals Co., Ltd.
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- August 9, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA207252
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Docetaxel | 20 mg/mL |
Drug Class
Microtubule Inhibition [PE]Microtubule Inhibitor [EPC]
Packaging Options(1)
1 VIAL, GLASS in 1 CARTON (57884-3041-1) / 1 mL in 1 VIAL, GLASS