Buminate - 0944-0490-01 - (Albumin Human)

Alphabetical Index


Drug Information of Buminate

Product NDC: 0944-0490
Proprietary Name: Buminate
Non Proprietary Name: Albumin Human
Active Ingredient(s): .25    g/mL & nbsp;   Albumin Human
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Buminate

Product NDC: 0944-0490
Labeler Name: Baxter Healthcare Corporation
Product Type: PLASMA DERIVATIVE
FDA Application Number: BLA101452
Marketing Category: BLA
Start Marketing Date: 19540317

Package Information of Buminate

Package NDC: 0944-0490-01
Package Description: 20 mL in 1 BOTTLE, GLASS (0944-0490-01)

NDC Information of Buminate

NDC Code 0944-0490-01
Proprietary Name Buminate
Package Description 20 mL in 1 BOTTLE, GLASS (0944-0490-01)
Product NDC 0944-0490
Product Type Name PLASMA DERIVATIVE
Non Proprietary Name Albumin Human
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19540317
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 Buminate


General Information