CORTIZEME EMULSION POUR APPLICATION CUTANEE
CORTIZEME EMULSION POUR APPLICATION CUTANEE
Authorised
- NEOMYCIN SULFATE
- Prednisolone
Product identification
Medicine name:
CORTIZEME EMULSION POUR APPLICATION CUTANEE
Active substance:
- NEOMYCIN SULFATE
- Prednisolone
Target species:
-
Dog
-
Cat
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
NEOMYCIN SULFATE5000.00/international unit(s)1.00millilitre(s)
-
Prednisolone1.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Cutaneous emulsion
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD07CA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Available in:
-
France
Package description:
- Available only in French
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/6326271 1/1990
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 31/03/2025
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 15/10/2025