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.
HumanVeterinaryMedicines

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:

Human medicines

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:

Topics

Share this page