Zycortal
desoxycortone
Table of contents
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.
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 |
Product information
20/08/2020 Zycortal - EMEA/V/C/003782 - R-0007
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:
- summary of product characteristics (annex I);
- manufacturing authorisation holder responsible for batch release (annex IIA);
- conditions of the marketing authorisation (annex IIB);
- labelling (annex IIIA);
- package leaflet (annex IIIB).
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).