BUSILVEX

This brand name is authorized in Austria, Brazil, Estonia, Finland, France, Ireland, Lithuania, Netherlands, Poland, South Africa, Spain, Turkey, UK.

Active ingredients

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

1
UNII G1LN9045DK - BUSULFAN
 

Busulfan is a potent cytotoxic agent and a bifunctional alkylating agent. In aqueous media, release of the methanesulphonate groups produces carbonium ions which can alkylate DNA, thought to be an important biological mechanism for its cytotoxic effect.

 
Read more about Busulfan

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 BUSILVEX Concentrate for solution MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

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

ATC Group Classification
L01AB01 Busulfan L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01A Alkylating agents → L01AB Alkyl sulfonates
Discover more medicines within L01AB01

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 507003901156311
EE Ravimiamet 1178254
ES Centro de información online de medicamentos de la AEMPS 03254002
FI Lääkealan turvallisuus- ja kehittämiskeskus 130309
FR Base de données publique des médicaments 65643325
GB Medicines & Healthcare Products Regulatory Agency 75334
LT Valstybinė vaistų kontrolės tarnyba 1027743, 1085238
NL Z-Index G-Standaard 15005933
NL Z-Index G-Standaard, PRK 129232
PL Rejestru Produktów Leczniczych 100126531
TR İlaç ve Tıbbi Cihaz Kurumu 8680683770029
ZA Health Products Regulatory Authority 37/26/0668

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