Medicinal Products

Opdivo

Name Opdivo
Active Substance nivolumab
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
ATC Code L01XC17
Medicinal product marketed in the Croatia Da
Educational materials
for healthcare professionals
Vodič za propisivanje, verzija 5
Educational materials
for patients / caregivers
Kartica s upozorenjima za bolesnika, verzija 4

Note

The medicinal product has been authorised via centralised procedure in all Member States of the European Union based on the European Medicines Agency's expert opinion. Additional information on the medicinal product can be found under the following link:https://www.ema.europa.eu/en/medicines/human/EPAR/opdivo

The marketing authorisation has been granted by the European Commission. All marketing authorisations of the European Commission can be found under the following link: http://ec.europa.eu/health/documents/community-register/html/index_en.htm

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