Paclitaxel 00781-3531
Product NDC
00781-3531- Manufacturer
- Sandoz Inc
- Dosage Form
- Injection, Powder, Lyophilized, For Suspension
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 8, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA212700
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Paclitaxel | 100 mg/20mL |
Drug Class
Microtubule Inhibitor [EPC]Microtubule Inhibition [PE]Microtubule Inhibitor [EPC]
Packaging Options(1)
1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3531-91) / 20 mL in 1 VIAL, SINGLE-DOSE