ADVATE - 0944-2922-02 - (Antihemophilic Factor, Human Recombinant)

Alphabetical Index


Drug Information of ADVATE

Product NDC: 0944-2922
Proprietary Name: ADVATE
Non Proprietary Name: Antihemophilic Factor, Human Recombinant
Active Ingredient(s):    & nbsp;   Antihemophilic Factor, Human Recombinant
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of ADVATE

Product NDC: 0944-2922
Labeler Name: Baxter Healthcare Corporation
Product Type: PLASMA DERIVATIVE
FDA Application Number: BLA125063
Marketing Category: BLA
Start Marketing Date: 20110204

Package Information of ADVATE

Package NDC: 0944-2922-02
Package Description: 1 KIT in 1 CARTON (0944-2922-02) * 1 VIAL, GLASS in 1 CARTON > 5 mL in 1 VIAL, GLASS * 2 mL in 1 VIAL, GLASS (52919-008-05)

NDC Information of ADVATE

NDC Code 0944-2922-02
Proprietary Name ADVATE
Package Description 1 KIT in 1 CARTON (0944-2922-02) * 1 VIAL, GLASS in 1 CARTON > 5 mL in 1 VIAL, GLASS * 2 mL in 1 VIAL, GLASS (52919-008-05)
Product NDC 0944-2922
Product Type Name PLASMA DERIVATIVE
Non Proprietary Name Antihemophilic Factor, Human Recombinant
Dosage Form Name KIT
Route Name
Start Marketing Date 20110204
Marketing Category Name BLA
Labeler Name Baxter Healthcare Corporation
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of ADVATE


General Information