National registers of authorised medicines

The national medicine registers in the different Member States of the European Union (EU) and European Economic Area (EEA) contain information on medicines authorised in those countries, including links for the summary of product characteristics (SmPC) and the package leaflet.

This complements information on medicines published on this website, which only includes medicines that the European Medicines Agency (EMA) evaluates.

Some of these registers cover both human and veterinary medicines.

To learn more about the different medicine authorisation routes in the EU, see:

•  Authorisation of medicines

Human medicines

Please note that the information in these national registers may not be available in English.

EU Member State	Medicine register
Austria	aspregister.basg.gv
Belgium	banquededonneesmedicaments.fagg-afmps.be/
Bulgaria	www.bda.bg (SmPC) www.bda.bg (package leaflet)
Croatia	www.halmed.hr
Cyprus	https://www.phs.moh.gov/cy
Czechia	www.sukl.eu
Denmark	www.laegemiddelstyrelsen.dk
Estonia	ravimiregister.ravimiamet.ee
Finland	www.fimea.fi
France	agence-prd.ansm.sante.fr
Germany	https://www.pharmnet-bund.de/PharmNet/DE/Oeffentlichkeit/Arzneimittel-Informationssystem/_node.html
Greece	www.eof.gr
Hungary	ogyei.gov.hu (human medicines) atiportal.nebih.gov.hu/ (veterinary medicines)
Ireland	www.hpra.ie
Italy	https://farmaci.agenziafarmaco.gov.it
Latvia	https://dati.zva.gov.lv
Lithuania	vapris.vvkt.lt
Luxembourg	No online register available
Malta	www.medicinesauthority.gov.mt
Netherlands	https://www.geneesmiddeleninformatiebank.nl/en
Poland	ezdrowie.gov.pl
Portugal	extranet.infarmed.pt
Romania	www.anm.ro
Slovakia	www.sukl.sk
Slovenia	www.cbz.si
Spain	cima.aemps.es
Sweden	www.lakemedelsverket.se
EEA Member State
Iceland	https://www.ima.is
Liechtenstein	See Austria
Norway	www.legemiddelsok.no

Veterinary medicines

The Coordination Group for Mutual Recognition and Decentralised Procedures for Veterinary Medicinal Products (CMDv) makes available a list of the national databases of authorised veterinary medicines from the Member States of the EU and EEA.

For more information:

• Head of Medicines Agencies - General information on applications (Further information)