NDC Code | 57884-3043-1 |
Package Description | 1 VIAL, GLASS in 1 CARTON (57884-3043-1) / 8 mL in 1 VIAL, GLASS |
Product NDC | 57884-3043 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Docetaxel |
Non-Proprietary Name | Docetaxel |
Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
Usage | INTRAVENOUS |
Start Marketing Date | 20170809 |
Marketing Category Name | ANDA |
Application Number | ANDA207252 |
Manufacturer | Jiangsu Hengrui Pharmaceuticals Co., Ltd. |
Substance Name | DOCETAXEL |
Strength | 160 |
Strength Unit | mg/8mL |
Pharmacy Classes | Microtubule Inhibition [PE], Microtubule Inhibitor [EPC] |