Product NDC: | 0053-8132 |
Proprietary Name: | Helixate FS |
Non Proprietary Name: | Antihemophilic Factor, Recombinant |
Active Ingredient(s): | & nbsp; Antihemophilic Factor, Recombinant |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0053-8132 |
Labeler Name: | CSL Behring LLC |
Product Type: | PLASMA DERIVATIVE |
FDA Application Number: | BLA103332 |
Marketing Category: | BLA |
Start Marketing Date: | 20000818 |
Package NDC: | 0053-8132-02 |
Package Description: | 1 KIT in 1 BOX (0053-8132-02) * 2.5 mL in 1 VIAL, SINGLE-USE (0053-8142-01) * 2.5 mL in 1 VIAL (0053-7653-52) |
NDC Code | 0053-8132-02 |
Proprietary Name | Helixate FS |
Package Description | 1 KIT in 1 BOX (0053-8132-02) * 2.5 mL in 1 VIAL, SINGLE-USE (0053-8142-01) * 2.5 mL in 1 VIAL (0053-7653-52) |
Product NDC | 0053-8132 |
Product Type Name | PLASMA DERIVATIVE |
Non Proprietary Name | Antihemophilic Factor, Recombinant |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20000818 |
Marketing Category Name | BLA |
Labeler Name | CSL Behring LLC |
Substance Name | |
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Strength Unit | |
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