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Rufinamide

Active substance: rufinamide

TABLET, FILM COATED · RUFINAMIDE 400 mg/1

United StatesActive

Marketing holder: Hikma Pharmaceuticals USA Inc.

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
EU 1
  • Inovelon
    rufinamide
    EMEA/H/C/000660
    Eisai GmbH
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-5b31-766f-b359-27179b228089,01a1208d-5249-7791-b9f7-0a1163ac770f,01a1208d-8d1b-7ce4-ad3c-199e2f4ce024,01a1208e-8b2b-7b7f-87c1-9f884b9196fc,01a1208e-a065-7992-936d-4f352918625b;count=24 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0054-0426
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0054-0426 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0054-0426 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0054-0426 · Verified 2026-10-09 · open in source