Medicinal Products

Hetlioz

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 Hetlioz
Active Substance tazimelteon
Prescription na recept
Type of prescription neponovljivi recept
Distribution u ljekarni
ATC Code N05CH03
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
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