This is a summary of the European public assessment report (EPAR) for NovoRapid. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use NovoRapid.
For practical information about using NovoRapid, patients should read the package leaflet or contact their doctor or pharmacist.
NovoRapid : EPAR - Summary for the public (PDF/75.99 KB)
First published: 06/08/2009
Last updated: 15/11/2016
|Agency product number||
|International non-proprietary name (INN) or common name||
|Therapeutic area (MeSH)||
|Anatomical therapeutic chemical (ATC) code||
Novo Nordisk A/S
|Date of issue of marketing authorisation valid throughout the European Union||
28/03/2019 NovoRapid - EMEA/H/C/000258 - N/0123
- Annex I - Summary of product characteristics
- Annex IIA - Manufacturing-authorisation holder responsible for batch release
- Annex IIB - Conditions of the marketing authorisation
- Annex IIIA - Labelling
- Annex IIIB - Package leaflet
Please note that the size of the above document can exceed 50 pages.
You are therefore advised to be selective about which sections or pages you wish to print.
Drugs used in diabetes
NovoRapid is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.