Vetoryl 30 mg chewable tablets for dogs
Vetoryl 30 mg chewable tablets for dogs
Authorised
- Trilostane
Product identification
Medicine name:
Vetoryl 30 mg chewable tablets for dogs
Vetoryl 30 mg chewable tablets for dogs
Active substance:
- Trilostane
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Trilostane30.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Chewable tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02CA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Aluminium – Polyamide/Aluminium/PVC blister.Each blister contains 10 tablets. Cardboard box of 1 blister.
- Aluminium – Polyamide/Aluminium/PVC blister.Each blister contains 10 tablets. Cardboard box of 3 blisters.
- Aluminium – Polyamide/Aluminium/PVC blister.Each blister contains 10 tablets. Cardboard box of 5 blisters.
- Aluminium – Polyamide/Aluminium/PVC blister.Each blister contains 10 tablets. Cardboard box of 6 blisters.
- Aluminium – Polyamide/Aluminium/PVC blister.Each blister contains 10 tablets. Cardboard box of 10 blisters.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - known active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Lelypharma B.V.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA22622/023/007
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0514/007
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
Czechia
-
Denmark
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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