Docetaxel 47335-0323
Product NDC
47335-0323- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- November 26, 2020
- Listing Expires
- December 31, 2026
- Application
- NDA022534
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Docetaxel Anhydrous | 20 mg/mL |
Drug Class
Microtubule Inhibitor [EPC]Microtubule Inhibition [PE]Microtubule Inhibitor [EPC]
Packaging Options(1)
1 VIAL, GLASS in 1 CARTON (47335-323-40) / 1 mL in 1 VIAL, GLASS