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EMA Product

Insulin lispro Sanofi

Product approved by European Medicines Agency (EU)

Basic Information

Insulin lispro Sanofi

Regulatory Information

EMEA/H/C/004303

Authorised

July 19, 2017

May 17, 2017

10

August 16, 2024

Company Information

France

82 Avenue Raspail 94250 Gentilly

SANOFI WINTHROP INDUSTRIE

Drug Classification

Biosimilar Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication For the treatment of adults and children with diabetes mellitus who require insulin for the maintenance of normal glucose homeostasis. Insulin lispro Sanofi is also indicated for the initial stabilisation of diabetes mellitus.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Insulin lispro Sanofi. 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 Insulin lispro Sanofi. For practical information about using Insulin lispro Sanofi, patients should read the package leaflet or contact their doctor or pharmacist.

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