Medicinal Products

Emtricitabine/Tenofovir disoproxil Mylan

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 Emtricitabine/Tenofovir disoproxil Mylan
Active Substance emtricitabin, tenofovirdizoproksilmaleat
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
ATC Code J05AR03
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 healthcare professionals
Lista provjere za propisivača, verzija 2
Edukacijska brošura za propisivače PrEP indikacija, verzija 3
HIV brošura za liječenje pedijatrijskih bolesnika za propisivače, verzija 4
Educational materials
for patients / caregivers
Edukacijska brošura za bolesnike, verzija 2
Kartica za korisnika lijeka, verzija 2
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