The marketing authorisation for RevitaCAM has been withdrawn at the request of the marketing authorisation holder.
RevitaCAM : EPAR - Summary for the public (PDF/689.07 KB)
First published: 14/03/2012
Last updated: 30/05/2016
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|International non-proprietary name (INN) or common name||
|Anatomical therapeutic chemical veterinary (ATCvet) codes||
This is a generic medicine, which is developed to be the same as a medicine that has already been authorised, called the reference medicine. A generic medicine contains the same active substance(s) as the reference medicine, and is used at the same dose(s) to treat the same disease(s). For more information, see Generic and hybrid medicines.
Zoetis Belgium SA
|Date of issue of marketing authorisation valid throughout the European Union||
05/10/2015 RevitaCAM - EMEA/V/C/002379 - T/0006
- 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
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Alleviation of inflammation and pain in both acute and chronic musculoskeletal disorders in dogs.