MedPath
EMA Product

Azilect

Product approved by European Medicines Agency (EU)

Basic Information

Azilect

Regulatory Information

EMEA/H/C/000574

Authorised

February 21, 2005

August 14, 2023

24

April 8, 2025

Company Information

the netherlands

Swensweg 5 2031GA Haarlem

Teva Pharma B.V.

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Azilect is indicated for the treatment of idiopathic Parkinson's disease (PD) as monotherapy (without levodopa) or as adjunct therapy (with levodopa) in patients with end-of-dose fluctuations.

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).

© Copyright 2025. All Rights Reserved by MedPath