AlbuRx - 44206-251-05 - (ALBUMIN (HUMAN))

Alphabetical Index


Drug Information of AlbuRx

Product NDC: 44206-251
Proprietary Name: AlbuRx
Non Proprietary Name: ALBUMIN (HUMAN)
Active Ingredient(s): 12.5    g/50mL & nbsp;   ALBUMIN (HUMAN)
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of AlbuRx

Product NDC: 44206-251
Labeler Name: CSL Behring AG
Product Type: PLASMA DERIVATIVE
FDA Application Number: BLA102366
Marketing Category: BLA
Start Marketing Date: 20090106

Package Information of AlbuRx

Package NDC: 44206-251-05
Package Description: 1 VIAL, GLASS in 1 CARTON (44206-251-05) > 50 mL in 1 VIAL, GLASS (44206-251-90)

NDC Information of AlbuRx

NDC Code 44206-251-05
Proprietary Name AlbuRx
Package Description 1 VIAL, GLASS in 1 CARTON (44206-251-05) > 50 mL in 1 VIAL, GLASS (44206-251-90)
Product NDC 44206-251
Product Type Name PLASMA DERIVATIVE
Non Proprietary Name ALBUMIN (HUMAN)
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090106
Marketing Category Name BLA
Labeler Name CSL Behring AG
Substance Name ALBUMIN (HUMAN)
Strength Number 12.5
Strength Unit g/50mL
Pharmaceutical Classes Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient]

Complete Information of AlbuRx


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