Albumin (Human) 20%

Name: Albumin (Human) 20%

Dosage Forms and Strengths

Albumin (Human) 20% is supplied in

  • 10 g in 50 mL infusion bottle
  • 20 g in 100 mL infusion bottle

Do not use in individuals who are hypersensitive to albumin preparations, any ingredient in the formulation, or components of the container.

Non-clinical toxicology

No non-clinical toxicology studies with Albumin (Human) 20% have been conducted. Human Albumin is a normal constituent of human plasma and acts like physiological albumin.

Package label - principal display panel

Albumin (Human) 20%

10 g in 50 mL

Octapharma Pharmazeutika Produktionsges.m.b.H

NDC 67467-633-01

Octapharma AB

NDC 68209-633-01

Albumin (Human) 20%

20 g in 100 mL

Octapharma Pharmazeutika Produktionsges.m.b.H

NDC 67467-633-02

Octapharma AB

NDC 68209-633-02

ALBUMIN (HUMAN) 
albumin human solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:67467-633
Route of Administration Intravenous DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALBUMIN (HUMAN) (ALBUMIN (HUMAN)) ALBUMIN (HUMAN) 200 g  in 1000 mL
Packaging
# Item Code Package Description
1 NDC:67467-633-01 50 mL in 1 BOTTLE, GLASS
2 NDC:67467-633-02 100 mL in 1 BOTTLE, GLASS
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA125154 10/17/2006
Labeler - Octapharma Pharmazeutika Produktionsgesellschaft m.b.H. (301119178)
Revised: 01/2010   Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
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