| NDC Code | 0955-1022-08 |
|---|
| Package Description | 1 VIAL, GLASS in 1 CARTON (0955-1022-08) / 8 mL in 1 VIAL, GLASS |
|---|
| Product NDC | 0955-1022 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Docetaxel |
|---|
| Non-Proprietary Name | Docetaxel |
|---|
| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20161023 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA020449 |
|---|
| Manufacturer | Winthrop U.S, a business of sanofi-aventis U.S. LLC |
|---|
| Substance Name | DOCETAXEL |
|---|
| Strength | 160 |
|---|
| Strength Unit | mg/8mL |
|---|
| Pharmacy Classes | Microtubule Inhibition [PE], Microtubule Inhibitor [EPC] |
|---|