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EMA Product

Izba

Product approved by European Medicines Agency (EU)

Basic Information

Izba

Regulatory Information

EMEA/H/C/002738

Authorised

February 20, 2014

8

November 29, 2021

Company Information

Ireland

Elm Park Merrion Road Dublin 4

NOVARTIS EUROPHARM LIMITED

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Decrease of elevated intraocular pressure in adult patients with ocular hypertension or open-angle glaucoma (see section 5.1). Decrease of elevated intraocular pressure in paediatric patients aged 3 years to < 18 years with ocular hypertension or paediatric glaucoma.

Overview Summary

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

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