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IMPORTANT NOTICE:

PLEASE NOTE THAT FROM 1 JANUARY 2021, AUTHORISATIONS IN ACCORDANCE WITH ARTICLE 126(A) AND PARALLEL IMPORT LICENCES GRANTED TO AA AND PI HOLDERS IN THE UNITED KINGDOM ARE NO LONGER VALID.  PARALLEL IMPORT LICENCES ON THE BASIS OF PRODUCTS AUTHORISED IN THE UNITED KINGDOM ARE NO LONGER VALID, IRRESPECTIVE OF THE PARALLEL IMPORT LICENCE HOLDER COUNTRY.  THE DATABASE WILL BE UPDATED IN THIS REGARD SHORTLY.


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Details of all the medicinal products authorised to be placed on the market in Malta together with the product information are available here.

The Medicines Authority is unable to offer medical advice and if a patient has any questions about a medicine they are taking, they should contact their doctor or pharmacist. Patients should not stop taking any prescribed medicines without first speaking to a healthcare professional. Suspected adverse reactions to a medicine can be reported to us on an ADR form.

Should you wish to have a full list of all products, select below whether you require a list of 'National Products' and an export of all products is created automatically. For centrally authorised products please refer to the European Medicines Agency.

Should you wish to search specific products or groups of products, please fill in this Advanced Search form and press Search.

For a list of recent product reclassifications of legal status (i.e. change in prescription status), please visit here.

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