Solriamfetol

SUNOSI 75 mg COMPRIMIDOS RECUBIERTOS CON PELICULA

89,25 mg comprimido recubierto con películaSpainMarketedAuthorised 12 Feb 2021

Product informationAsk Osler about it

In other countries

The same active substances on other registers, the same brand first.

Authorised centrally in the EU

This national listing belongs to a medicine the European Commission authorised for the whole EU.

SunosiEuropean UnionAuthorised

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Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

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Solriamfetol

SUNOSI 75 mg COMPRIMIDOS RECUBIERTOS CON PELICULA

89,25 mg comprimido recubierto con películaSpainMarketedAuthorised 12 Feb 2021

Product informationAsk Osler about it

In other countries

The same active substances on other registers, the same brand first.

Authorised centrally in the EU

This national listing belongs to a medicine the European Commission authorised for the whole EU.

SunosiEuropean UnionAuthorised

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

Discover Osler

Sunosi 300 mg filmomhulde tablettenNetherlands · Filmomhulde tablet · Atnahs Pharma Netherlands B.V.

Sunosi 75 mg filmomhulde tablettenNetherlands · Filmomhulde tablet · Atnahs Pharma Netherlands B.V.

SunosiUnited States · 150MG BASE, 75MG BASE · tablet · Axsome Malta

SolriamfetolUnited States · 150MG, 300MG, 75MG · tablet · Aurobindo Pharma Limited

Packs

Pack	Code	Status
SUNOSI 75 mg COMPRIMIDOS RECUBIERTOS CON PELICULA, 28 comprimidos	730054

Documents

The official texts, at the regulator.

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

Agencia Española de Medicamentos y Productos Sanitarios

Fuente de la información: Agencia Española de Medicamentos y Productos Sanitarios www.aemps.gob.es; CIMA medicamentos, acquired 11 October 2026 UTC; each source response/update date retained.

Licence: AEMPS explicit public open-data reuse for citizens and companies; source attribution and update date required · Added 12 Oct 2026

Report an error or request removalCorrections from the holder or the register are welcome.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Active substance: Solriamfetol
Strength: 89,25 mg
Dosage form: comprimido recubierto con película
Route: vía oral
Register: Spain (AEMPS)
Status: Marketed
Status in the register: Autorizado, comercializado
Authorised: 12 Feb 2021
Registration: 1191408002
Marketing authorisation holder: Atnahs Pharma Netherlands Bv.
Procedure: EU centralised
Supply: Diagnóstico Hospitalario
EU number: EU/1/19/1408