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EMA Product

Apidra

Product approved by European Medicines Agency (EU)

Basic Information

Apidra

Regulatory Information

EMEA/H/C/000557

Authorised

September 27, 2004

June 3, 2004

34

August 9, 2024

Company Information

Germany

Sanofi-Aventis Deutschland GmbH Brueningstrasse 50, D-65926 Frankfurt am Main

Sanofi-Aventis Deutschland Gmbh

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of adults, adolescents and children, six years or older with diabetes mellitus, where treatment with insulin is required.

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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