NDC Code | 0955-1727-20 |
Package Description | 1 VIAL, GLASS in 1 CARTON (0955-1727-20) / 20 mL in 1 VIAL, GLASS |
Product NDC | 0955-1727 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Oxaliplatin |
Non-Proprietary Name | Oxaliplatin |
Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
Usage | INTRAVENOUS |
Start Marketing Date | 20140707 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA021759 |
Manufacturer | Winthrop U.S, a business of sanofi-aventis U.S. LLC |
Substance Name | OXALIPLATIN |
Strength | 5 |
Strength Unit | mg/mL |
Pharmacy Classes | Platinum-based Drug [EPC], Platinum-containing Compounds [EXT] |