Medicinal Products

Neulasta

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 Neulasta
Active Substance pegfilgrastim
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
ATC Code L03AA13
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
Neulasta OBI kartica za bolesnika, verzija 1
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