DESFERAL

This brand name is authorized in United States. It is also authorized in Austria, Brazil, Canada, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Japan, Lithuania, Malta, Netherlands, Poland, Romania, Tunisia, Turkey, UK.

Active ingredients

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

1
UNII V9TKO7EO6K - DEFEROXAMINE MESYLATE
 

Deferoxamine is a chelating agent for trivalent iron and aluminium ions. The resulting chelates are stable and non-toxic.

 
Read more about Deferoxamine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 DESFERAL Sterile, lyophilised powder MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
V03AC01 Deferoxamine V Various → V03 All other therapeutic products → V03A All other therapeutic products → V03AC Iron chelating agents
Discover more medicines within V03AC01

Authorization and marketing

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 526504501157411
CA Health Products and Food Branch 01981242
EE Ravimiamet 1116526, 1636725, 1784628, 1832442, 1866517, 1870152
FI Lääkealan turvallisuus- ja kehittämiskeskus 189175
FR Base de données publique des médicaments 68537836
GB Medicines & Healthcare Products Regulatory Agency 142247, 37580
HK Department of Health Drug Office 06780, 64622
IL מִשְׂרַד הַבְּרִיאוּת 528
IT Agenzia del Farmaco 020417022
JP 医薬品医療機器総合機構 3929402D1036
LT Valstybinė vaistų kontrolės tarnyba 1090536, 1090640
MT Medicines Authority MA1249/02201
NL Z-Index G-Standaard, PRK 795
PL Rejestru Produktów Leczniczych 100018155, 100330929, 100446974, 100456091
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W02408001
TN Direction de la Pharmacie et du Médicament 10283161H
TR İlaç ve Tıbbi Cihaz Kurumu 8699504790108
US FDA, National Drug Code 0078-0467

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