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RECOMBINATE - 0944-2841-10 - (Antihemophilic Factor Recombinant)

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Drug Information of RECOMBINATE

Product NDC: 0944-2841
Proprietary Name: RECOMBINATE
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)

Labeler Information of RECOMBINATE

Product NDC: 0944-2841
Labeler Name: Baxter Healthcare Corporation
Product Type: PLASMA DERIVATIVE
FDA Application Number: BLA103375
Marketing Category: BLA
Start Marketing Date: 19921210

Package Information of RECOMBINATE

Package NDC: 0944-2841-10
Package Description: 1 KIT in 1 CARTON (0944-2841-10) * 10 mL in 1 VIAL, GLASS (0944-2831-01) * 5 mL in 1 VIAL, GLASS (52919-003-08)

NDC Information of RECOMBINATE

NDC Code 0944-2841-10
Proprietary Name RECOMBINATE
Package Description 1 KIT in 1 CARTON (0944-2841-10) * 10 mL in 1 VIAL, GLASS (0944-2831-01) * 5 mL in 1 VIAL, GLASS (52919-003-08)
Product NDC 0944-2841
Product Type Name PLASMA DERIVATIVE
Non Proprietary Name Antihemophilic Factor Recombinant
Dosage Form Name KIT
Route Name
Start Marketing Date 19921210
Marketing Category Name BLA
Labeler Name Baxter Healthcare Corporation
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of RECOMBINATE


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