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Multaq

Active substance: dronedarone

TABLET, FILM COATED · DRONEDARONE 400 mg/1

United StatesActive

Marketing holder: Sanofi-Aventis U.S. LLC

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 2
  • Multaq
    dronedarone
    EMEA/H/C/001043
    Sanofi Winthrop Industrie
  • Multaq
    dronedarone
    EMEA/H/C/000676
    Sanofi-Aventis
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-7b6e-7f79-b100-02e0fc296ce9,01a1209b-3889-7645-9720-c5b040eb34d7;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0024-4142
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0024-4142 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0024-4142 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0024-4142 · Verified 2026-10-09 · open in source