Docetaxel 70121-1222
Product NDC
70121-1222- Manufacturer
- Amneal Pharmaceuticals Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- January 19, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA209640
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Docetaxel Anhydrous | 80 mg/4mL |
Drug Class
Microtubule Inhibitor [EPC]Microtubule Inhibition [PE]Microtubule Inhibitor [EPC]
Packaging Options(1)
1 VIAL, GLASS in 1 CARTON (70121-1222-1) / 4 mL in 1 VIAL, GLASS