PLASBUMIN

This brand name is authorized in United States. It is also authorized in Canada, Cyprus, Hong Kong SAR China, Singapore, Spain, Turkey.

Active ingredients

The drug PLASBUMIN contains one active pharmaceutical ingredient (API):

1
UNII ZIF514RVZR - ALBUMIN HUMAN
 

Human albumin accounts quantitatively for more than half of the total protein in the plasma and represents about 10% of the protein synthesis activity of the liver. The most important physiological functions of albumin results from its contribution to oncotic pressure of the blood and transport function. Albumin stabilises circulating blood volume and is a carrier of hormones, enzymes, medicinal products and toxins.

 
Read more about Albumin

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
B05AA01 Albumin B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05A Blood and related products → B05AA Blood substitutes and plasma protein fractions
Discover more medicines within B05AA01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02189100
ES Centro de información online de medicamentos de la AEMPS 61499
HK Department of Health Drug Office 06008
SG Health Sciences Authority 01972P
TR İlaç ve Tıbbi Cihaz Kurumu 8699769980269, 8699769980276, 8699769980283, 8699769980290
US FDA, National Drug Code 13533-690, 13533-691, 13533-692

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