Medicinal Products

Ledaga

The medicinal product has been authorised by the European Commission (EC) via centralised procedure in all EU Member States, based on the European Medicines Agency (EMA) experts' opinion.

Name Ledaga
Active Substance klormetin
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
ATC Code L01AA05
Summary of product characteristics (SmPC), labelling and package leaflet (PL) download
Link to the European Medicines Agency's (EMA) product information download
Link to the European Commission's (EC) decisions download
Educational materials
for patients / caregivers
Upozorenje za bolesnike na pakiranju lijeka
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