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Sunosi

Active substance: solriamfetol

solriamfetol hydrochloride

Centralised EU authorisationActive

Marketing holder: Atnahs Pharma Netherlands B.V.

Verified 2026-10-09 · EMA

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
US 2
  • SUNOSI
    TABLET, FILM COATED · SOLRIAMFETOL 75 mg/1
    81968-350
    Axsome Therapeutics, Inc.
  • SUNOSI
    TABLET, FILM COATED · SOLRIAMFETOL 150 mg/1
    81968-351
    Axsome Therapeutics, Inc.
Import and control

Control by country

  • United StatescontrolledSchedule: CIV

    Source: openFDA NDC · record 01a12091-106a-7abe-96cd-c527cf98c7b9,01a1209a-2594-7cc7-96bb-1d0717eb5501;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/004893
Registration status
Active
ATC code
N06BA14
Sources
  • product · EMA · EMEA/H/C/004893 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/004893 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/004893 · Verified 2026-10-09