United States · FDA National Drug Code directory
Banzel
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 62856-582_0cc6f13a-0289-45f7-980e-3196d7489d75
- Product NDC
- 62856-582
- Form
- TABLET, FILM COATED
- Composition / generic term
- rufinamide
- Labeler
- Eisai Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20081114
- Source listing expiry
- 20261231
Source-listed ingredients
- RUFINAMIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET, FILM COATED in 1 BOTTLE (62856-582-04) · 62856-582-04
- 120 TABLET, FILM COATED in 1 BOTTLE (62856-582-52) · 62856-582-52
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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