This is a summary of the European public assessment report (EPAR) for Imrestor. It explains how the Agency assessed this veterinary medicine to recommend its authorisation in the European Union (EU) and its conditions of use. It is not intended to provide practical advice on how to use Imrestor.
For practical information about using Imrestor, animal owners or keepers should read the package leaflet or contact their veterinarian or pharmacist.
Imrestor : EPAR - Summary for the public (PDF/78.18 KB)
First published: 01/04/2016
Last updated: 01/04/2016
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13/12/2019 Imrestor - EMEA/V/C/002763 - IAIN/0011/G
- Annex I - Summary of product characteristics
- Annex IIA - Manufacturing-authorisation holder responsible for batch release
- Annex IIB - Conditions of the marketing authorisation
- Annex IIIA - Labelling
- Annex IIIB - Package leaflet
Please note that the size of the above document can exceed 50 pages.
You are therefore advised to be selective about which sections or pages you wish to print.
As an aid in a herd management programme, to reduce the risk of clinical mastitis in periparturient dairy cows and heifers during the 30 days following calving.