Exzolt

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fluralaner

Authorised
This medicine is authorised for use in the European Union.

Overview

This is a summary of the European public assessment report (EPAR) for Exzolt.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 Exzolt.

For practical information about using Exzolt, animal owners or keepers should read the package leaflet or contact their veterinarian or pharmacist.

This EPAR was last updated on 12/01/2022

Authorisation details

Product details
Name
Exzolt
Agency product number
EMEA/V/C/004344
Active substance
fluralaner
International non-proprietary name (INN) or common name
fluralaner
Species
Chicken
Anatomical therapeutic chemical veterinary (ATCvet) codes
QP53BE02
Publication details
Marketing-authorisation holder
Intervet International B.V.
Revision
3
Date of issue of marketing authorisation valid throughout the European Union
18/08/2017
Contact address

Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands

Product information

22/12/2021 Exzolt - EMEA/V/C/004344 - IB-0013

Other EU languages available icon This medicine’s product information is available in all official EU languages.
Select ‘available languages’ to access the language you need.

 

Product information documents contain:

You can find product information documents for centrally authorised human medicines on this website. For centrally authorised veterinary medicines authorised or updated from February 2022, see the Veterinary Medicines Information website.

Pharmacotherapeutic group

Ectoparaciticides, insecticides and repellents

Therapeutic indication

Treatment of poultry red mite (Dermanyssus gallinae) infestation in pullets, breeders and layer hens.

Assessment history

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