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EMA Product

Odomzo

Product approved by European Medicines Agency (EU)

Basic Information

Odomzo

Regulatory Information

EMEA/H/C/002839

Authorised

August 14, 2015

June 25, 2015

10

April 26, 2021

Company Information

the netherlands

Polarisavenue 87 2132JH Hoofddorp

Sun Pharmaceutical Industries (Europe) B.V.

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Odomzo is indicated for the treatment of adult patients with locally advanced basal cell carcinoma (BCC) who are not amenable to curative surgery or radiation therapy.

Overview Summary

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

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