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EMA Product

Elmiron

Product approved by European Medicines Agency (EU)

Basic Information

Elmiron

Regulatory Information

EMEA/H/C/004246

Authorised

June 2, 2017

14

July 15, 2022

Company Information

Germany

Herterichstrasse 1-3 81479 Munich

bene-Arzneimittel GmbH

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Elmiron is indicated for the treatment of bladder pain syndrome characterized by either glomerulations or Hunner’s lesions in adults with moderate to severe pain, urgency and frequency of micturition.

Overview Summary

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

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