This brand name is authorized in Austria, Brazil, Canada, Cyprus, Finland, France, Ireland, Malta, Netherlands, Poland, Romania, Spain, Turkey, UK.
The drug ALBUREX contains one active pharmaceutical ingredient (API):
1
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UNII
ZIF514RVZR - ALBUMIN HUMAN
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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. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| ALBUREX 20, 200g/l Solution for infusion | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) | |
| ALBUREX 5, 50 g/l Solution for infusion | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
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 |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| BR | Câmara de Regulação do Mercado de Medicamentos | 502601804153413 |
| CA | Health Products and Food Branch | 02274655, 02274663 |
| ES | Centro de información online de medicamentos de la AEMPS | 71692, 71694 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 078205, 078216, 415202 |
| FR | Base de données publique des médicaments | 63124513 |
| GB | Medicines & Healthcare Products Regulatory Agency | 215924, 215925 |
| MT | Medicines Authority | MA665/00901, MA665/00902, MA665/00903, MA665/00904, MA665/00905 |
| NL | Z-Index G-Standaard, PRK | 24082, 69663 |
| PL | Rejestru Produktów Leczniczych | 100233729, 100233758 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W55304001, W55304002, W55304003, W55305001, W55305002 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8681624980248, 8681624980255 |
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