NDC 31722-599 – Rufinamide

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

Human Prescription Drug

Product NDC31722-599

Product details

Brand name
Rufinamide
Generic name
Rufinamide
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204993
Marketed since
May 11, 2021
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Rufinamide →

Package NDC codes (2)

Package NDCDescriptionSince
31722-599-12120 TABLET, FILM COATED in 1 BOTTLE (31722-599-12)May 11, 2021
31722-599-3030 TABLET, FILM COATED in 1 BOTTLE (31722-599-30)May 11, 2021

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