NDC Code | 78206-162-01 |
Package Description | 1 VIAL in 1 CARTON (78206-162-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (78206-162-99) |
Product NDC | 78206-162 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Renflexis |
Non-Proprietary Name | Infliximab |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20170421 |
Marketing Category Name | BLA |
Application Number | BLA761054 |
Manufacturer | Organon LLC |
Substance Name | INFLIXIMAB |
Strength | 100 |
Strength Unit | mg/1 |
Pharmacy Classes | Tumor Necrosis Factor Blocker [EPC], Tumor Necrosis Factor Receptor Blocking Activity [MoA] |