NDC 62856-583 – Banzel

Rufinamide 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC62856-583

Product details

Brand name
Banzel
Generic name
Rufinamide
Labeler
Eisai Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA021911
Marketed since
November 14, 2008
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Banzel →

Package NDC codes (2)

Package NDCDescriptionSince
62856-583-14 sample14 TABLET, FILM COATED in 1 BOTTLE (62856-583-14)Aug 8, 2018
62856-583-52120 TABLET, FILM COATED in 1 BOTTLE (62856-583-52)Nov 14, 2008

Recalls mentioning this NDC

Other Banzel products