Medicinal Products

Enbrel

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 Enbrel
Active Substance etanercept
Prescription na recept
Type of prescription ograničeni recept (prašak i otapalo za otopinu za injekciju, prašak za otopinu za injekciju, otopina za injekciju u napunjenoj štrcaljki, otopina za injekciju u napunjenoj brizgalici, prašak i otapalo za otopinu za injekciju za pedijatrijsku primjenu)
Distribution u ljekarni
ATC Code L04AB01
Medicinal product marketed in the Croatia Da
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
Kartica za bolesnika
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