Pruban

RSS

resocortol butyrate

Withdrawn
This medicine is now withdrawn from use in the European Union.

Overview

The marketing authorisation for Pruban has not been renewed by the marketing authorisation holder and is now withdrawn.

This EPAR was last updated on 26/07/2010

Authorisation details

Product details
Name
Pruban
Agency product number
EMEA/V/C/000048
Active substance
resocortol butyrate
International non-proprietary name (INN) or common name
resocortol butyrate
Species
Dogs
Anatomical therapeutic chemical veterinary (ATCvet) codes
QD07AC90
Publication details
Marketing-authorisation holder
Intervet International BV
Revision
4
Date of issue of marketing authorisation valid throughout the European Union
16/11/2000
Contact address
Intervet International B.V.
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands

Product information

14/06/2010 Pruban - EMEA/V/C/000048 - R/0004

Contents

  • 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.

Pharmacotherapeutic group

Corticosteroids, dermatological preparations

Therapeutic indication

Treatment of acute localised moist dermatitis.

Assessment history

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