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EMA Product

Ritonavir Viatris (previously Ritonavir Mylan)

Product approved by European Medicines Agency (EU)

Basic Information

Ritonavir Viatris (previously Ritonavir Mylan)

Regulatory Information

EMEA/H/C/004549

Authorised

November 9, 2017

September 14, 2017

17

September 11, 2024

Company Information

Ireland

Damastown Industrial Park Dublin 15

VIATRIS PHARMA LIMITED

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Ritonavir is indicated in combination with other antiretroviral agents for the treatment of HIV 1 infected patients (adults and children of 2 years of age and older).

Overview Summary

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

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