Product NDC: | 63833-891 |
Proprietary Name: | RiaSTAP |
Non Proprietary Name: | Fibrinogen |
Active Ingredient(s): | 1300 mg/50mL & nbsp; Fibrinogen |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63833-891 |
Labeler Name: | CSL Behring GmbH |
Product Type: | PLASMA DERIVATIVE |
FDA Application Number: | BLA125317 |
Marketing Category: | BLA |
Start Marketing Date: | 20090116 |
Package NDC: | 63833-891-51 |
Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (63833-891-51) > 50 mL in 1 VIAL, SINGLE-USE |
NDC Code | 63833-891-51 |
Proprietary Name | RiaSTAP |
Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (63833-891-51) > 50 mL in 1 VIAL, SINGLE-USE |
Product NDC | 63833-891 |
Product Type Name | PLASMA DERIVATIVE |
Non Proprietary Name | Fibrinogen |
Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20090116 |
Marketing Category Name | BLA |
Labeler Name | CSL Behring GmbH |
Substance Name | FIBRINOGEN |
Strength Number | 1300 |
Strength Unit | mg/50mL |
Pharmaceutical Classes | Human Blood Coagulation Factor [EPC],Increased Coagulation Activity [PE],Blood Coagulation Factors [Chemical/Ingredient] |