BUSILVEX

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

Active ingredients

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

1 Busulfan
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 about Busulfan

Medication package inserts

Below package inserts are available for further reading:

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

Medicine classification

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

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

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