This brand name is authorized in United States. It is also authorized in Canada.
The drug BANZEL contains one active pharmaceutical ingredient (API):
1
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UNII
WFW942PR79 - RUFINAMIDE
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Rufinamide is an anticonvulsant medication. Rufinamide modulates the activity of sodium channels, prolonging their inactive state. |
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Below package inserts are available for further reading:
Document | Type | Information Source | |
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BANZEL Film-coated tablet / Oral suspension | MPI, US: SPL/PLR | FDA, National Drug Code (US) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC Group | Classification | |
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N03AF03 | Rufinamide | N Nervous system → N03 Antiepileptics → N03A Antiepileptics → N03AF Carboxamide derivatives |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
CA | Health Products and Food Branch | 02369613, 02369621, 02369648 |
US | FDA, National Drug Code | 62856-582, 62856-583, 62856-584 |
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