Vidalta 15 mg prolonged-release tablets for cats
Vidalta 15 mg prolonged-release tablets for cats
Authorised
- Carbimazole
Product identification
Medicine name:
Vidalta 15 mg prolonged-release tablets for cats
VIDALTA 15 MG COMPRIMES A LIBERATION PROLONGEE POUR CHATS
Active substance:
- Carbimazole
Target species:
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Carbimazole15.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH03BB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- High density polyethylene container of 100 tablets closed with polypropylene tamper-evident, child-resistant, screw cap bearing a desiccant.
- High density polyethylene container of 30 closed with polypropylene tamper-evident, child-resistant, screw cap bearing a desiccant.
- 6 high density polyethylene containers of 30 closed with polypropylene tamper-evident, child-resistant, screw cap bearing a desiccant.
- 6 High density polyethylene containers of 100 tablets closed with polypropylene tamper-evident, child-resistant, screw cap bearing a desiccant.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet Ges.m.b.H.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/8824284 4/2011
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0442/002
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Denmark
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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