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EMA Product

Insulin aspart Sanofi

Product approved by European Medicines Agency (EU)

Basic Information

Insulin aspart Sanofi

Regulatory Information

EMEA/H/C/005033

Authorised

June 25, 2020

April 30, 2020

6

September 23, 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 Insulin aspart Sanofi is indicated for the treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.

Overview Summary

Insulin aspart Sanofi is a medicine used to control blood glucose (sugar) levels in patients from one year of age who have diabetes. Insulin aspart Sanofi is a ‘biosimilar medicine’. This means that Insulin aspart Sanofi is highly similar to another biological medicine (the ‘reference medicine’) that is already authorised in the EU. The reference medicine for Insulin aspart Sanofi is NovoRapid. Insulin aspart Sanofi contains the active substance insulin aspart, a rapid-acting insulin.

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