RiaSTAP - 63833-891-51 - (Fibrinogen)

Alphabetical Index


Drug Information of RiaSTAP

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)

Labeler Information of RiaSTAP

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 Information of RiaSTAP

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 Information of RiaSTAP

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]

Complete Information of RiaSTAP


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