National registers of authorised medicines

The European Medicines Agency (EMA) has compiled a list of national medicine registers in the different Member States of the European Union (EU) and European Economic Area (EEA). These contain information on medicines authorised in those countries, including links for the summary of product characteristics (SmPC) and the package leaflet. Some of these registers cover both human and veterinary medicines.

This complements information on medicines published on EMA's website, which only includes medicines EMA evaluates.

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.produktresume.dk
Estonia	ravimiregister.ravimiamet.ee
Finland	www.fimea.fi
France	agence-prd.ansm.sante.fr
Germany	www.pharmnet-bund.de
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