Zycortal

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desoxycortone

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

Overview

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

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

This EPAR was last updated on 23/04/2019

Authorisation details

Product details
Name
Zycortal
Agency product number
EMEA/V/C/003782
Active substance
desoxycortone pivalate
International non-proprietary name (INN) or common name
desoxycortone
Species
Dogs
Anatomical therapeutic chemical veterinary (ATCvet) codes
QH02AA03
Publication details
Marketing-authorisation holder
Dechra Regulatory B.V.
Revision
3
Date of issue of marketing authorisation valid throughout the European Union
06/11/2015
Contact address

Handelsweg 25
5531 AE Bladel
The Netherlands

Product information

09/04/2019 Zycortal - EMEA/V/C/003782 - IAIN-0006-G

Contents

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.

Pharmacotherapeutic group

CORTICOSTEROIDS FOR SYSTEMIC USE

Therapeutic indication

For use as replacement therapy for mineralocorticoid deficiency in dogs with primary hypoadrenocorticism (Addison's disease).

Assessment history

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