Rufinamide

NDC 31722-599 · Camber Pharmaceuticals, Inc.

Generic nameRufinamide

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)RUFINAMIDE

Strength400 mg/1

Marketing categoryANDA

Packages

31722-599-12 — 120 TABLET, FILM COATED in 1 BOTTLE (31722-599-12)

31722-599-30 — 30 TABLET, FILM COATED in 1 BOTTLE (31722-599-30)

FDA lists these products with the same active ingredient.

0054-0425 — Rufinamide, 0054-0426 — Rufinamide, 0054-0528 — Rufinamide, 31722-598 — Rufinamide, 31722-688 — Rufinamide, 42571-391 — RUFINAMIDE, 42571-392 — RUFINAMIDE, 59651-563 — RUFINAMIDE, 59651-616 — rufinamide, 59651-617 — rufinamide, 60687-824 — Rufinamide, 62856-582 — rufinamide, 62856-583 — rufinamide, 62856-584 — rufinamide, 67877-673 — Rufinamide, 68180-797 — Rufinamide, 68180-803 — rufinamide, 68180-804 — rufinamide, 68462-713 — rufinamide, 68462-714 — rufinamide, +3 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.