This brand name is authorized in Austria, Brazil, Estonia, Spain, Finland, France, Ireland, Lithuania, Netherlands, Poland, Turkey, United Kingdom, South Africa
The drug BUSILVEX contains one active pharmaceutical ingredient (API):
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1
Busulfan
UNII G1LN9045DK - BUSULFAN
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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. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| BUSILVEX Concentrate for solution | European Medicines Agency (EU) | MPI, EU: SmPC |
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 |
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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