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EMA Product

Rasagiline Mylan

Product approved by European Medicines Agency (EU)

Basic Information

Rasagiline Mylan

Regulatory Information

EMEA/H/C/004064

Authorised

April 4, 2016

January 28, 2016

10

May 13, 2024

Company Information

Ireland

Damastown Industrial Park Mulhuddart Dublin 15

VIATRIS PHARMA LIMITED

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Rasagiline Mylan 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) for Rasagiline Mylan. 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 Rasagiline Mylan. For practical information about using Rasagiline Mylan, patients should read the package leaflet or contact their doctor or pharmacist.

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