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EMA Product

Memantine Accord

Product approved by European Medicines Agency (EU)

Basic Information

Memantine Accord

Regulatory Information

EMEA/H/C/002766

Authorised

December 3, 2013

September 18, 2013

7

January 12, 2022

Company Information

Spain

Edificio Este Planta 6a World Trade Center Moll De Barcelona S/n 08039 Barcelona

ACCORD HEALTHCARE SL

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of patients with moderate to severe Alzheimer’s disease.

Overview Summary

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

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