FLEXBUMIN - 0944-0493-02 - (Albumin Human)

Alphabetical Index


Drug Information of FLEXBUMIN

Product NDC: 0944-0493
Proprietary Name: FLEXBUMIN
Non Proprietary Name: Albumin Human
Active Ingredient(s): .25    g/mL & nbsp;   Albumin Human
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of FLEXBUMIN

Product NDC: 0944-0493
Labeler Name: Baxter Healthcare Corporation
Product Type: PLASMA DERIVATIVE
FDA Application Number: BLA101452
Marketing Category: BLA
Start Marketing Date: 20020809

Package Information of FLEXBUMIN

Package NDC: 0944-0493-02
Package Description: 100 mL in 1 BAG (0944-0493-02)

NDC Information of FLEXBUMIN

NDC Code 0944-0493-02
Proprietary Name FLEXBUMIN
Package Description 100 mL in 1 BAG (0944-0493-02)
Product NDC 0944-0493
Product Type Name PLASMA DERIVATIVE
Non Proprietary Name Albumin Human
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20020809
Marketing Category Name BLA
Labeler Name Baxter Healthcare Corporation
Substance Name ALBUMIN (HUMAN)
Strength Number .25
Strength Unit g/mL
Pharmaceutical Classes Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient]

Complete Information of FLEXBUMIN


General Information