Product NDC: | 0169-7040 |
Proprietary Name: | NovoSeven |
Non Proprietary Name: | Coagulation Factor VIIa (Recombinant) |
Active Ingredient(s): | & nbsp; Coagulation Factor VIIa (Recombinant) |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0169-7040 |
Labeler Name: | Novo Nordisk |
Product Type: | PLASMA DERIVATIVE |
FDA Application Number: | BLA103665 |
Marketing Category: | BLA |
Start Marketing Date: | 20100806 |
Package NDC: | 0169-7040-01 |
Package Description: | 1 KIT in 1 KIT (0169-7040-01) * 8.1 mL in 1 VIAL, GLASS * 8.1 mL in 1 VIAL, GLASS |
NDC Code | 0169-7040-01 |
Proprietary Name | NovoSeven |
Package Description | 1 KIT in 1 KIT (0169-7040-01) * 8.1 mL in 1 VIAL, GLASS * 8.1 mL in 1 VIAL, GLASS |
Product NDC | 0169-7040 |
Product Type Name | PLASMA DERIVATIVE |
Non Proprietary Name | Coagulation Factor VIIa (Recombinant) |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100806 |
Marketing Category Name | BLA |
Labeler Name | Novo Nordisk |
Substance Name | |
Strength Number | |
Strength Unit | |
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