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EMA Product

Mixtard

Product approved by European Medicines Agency (EU)

Basic Information

Mixtard

Regulatory Information

EMEA/H/C/000428

Authorised

October 7, 2002

April 25, 2002

20

January 24, 2024

Company Information

Denmark

Novo Allé DK-2880 Bagsvaerd

Novo Nordisk A/S

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of diabetes mellitus.

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal products for Human Use (CHMP) assessed the studies performed, to reach its recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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