NDC Code | 57894-421-01 |
Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (57894-421-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE |
Product NDC | 57894-421 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Sylvant |
Non-Proprietary Name | Siltuximab |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20140401 |
End Marketing Date | 20210131 |
Marketing Category Name | BLA |
Application Number | BLA125496 |
Manufacturer | Janssen Biotech, Inc. |
Substance Name | SILTUXIMAB |
Strength | 400 |
Strength Unit | mg/1 |
Pharmacy Classes | Interleukin-6 Antagonist [EPC],Interleukin-6 Antagonists [MoA] |