Docetaxel 71288-0152
Product NDC
71288-0152- Manufacturer
- Meitheal Pharmaceuticals Inc.
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- May 13, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA213768
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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, SINGLE-DOSE in 1 CARTON (71288-152-04) / 4 mL in 1 VIAL, SINGLE-DOSE