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 27/08/2020

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
4
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

20/08/2020 Zycortal - EMEA/V/C/003782 - R-0007

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

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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