Albuked - 76125-784-20 - (Albumin (Human))

Alphabetical Index


Drug Information of Albuked

Product NDC: 76125-784
Proprietary Name: Albuked
Non Proprietary Name: Albumin (Human)
Active Ingredient(s): 5    g/20mL & nbsp;   Albumin (Human)
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Albuked

Product NDC: 76125-784
Labeler Name: KEDRION BIOPHARMA, INC
Product Type: PLASMA DERIVATIVE
FDA Application Number: BLA101138
Marketing Category: BLA
Start Marketing Date: 19421021

Package Information of Albuked

Package NDC: 76125-784-20
Package Description: 1 VIAL in 1 CARTON (76125-784-20) > 20 mL in 1 VIAL (76125-784-21)

NDC Information of Albuked

NDC Code 76125-784-20
Proprietary Name Albuked
Package Description 1 VIAL in 1 CARTON (76125-784-20) > 20 mL in 1 VIAL (76125-784-21)
Product NDC 76125-784
Product Type Name PLASMA DERIVATIVE
Non Proprietary Name Albumin (Human)
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19421021
Marketing Category Name BLA
Labeler Name KEDRION BIOPHARMA, INC
Substance Name ALBUMIN (HUMAN)
Strength Number 5
Strength Unit g/20mL
Pharmaceutical Classes Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient]

Complete Information of Albuked


General Information