KESIUM 500 MG / 125 MG CHEWABLE TABLETS FOR DOGS
KESIUM 500 MG / 125 MG CHEWABLE TABLETS FOR DOGS
Authorised
- Amoxicillin trihydrate
- Potassium clavulanate
Product identification
Medicine name:
KESIUM 500 MG / 125 MG CHEWABLE TABLETS FOR DOGS
Kesium 500 mg - 125 mg Kauwtablet
Kesium 500 mg - 125 mg Comprimé à croquer
Kesium 500 mg - 125 mg Kautablette
Active substance:
- Amoxicillin trihydrate
- Potassium clavulanate
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate574.00milligram(s)1.00Tablet
-
Potassium clavulanate149.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Chewable tablet
Withdrawal period by route of administration:
-
Oral use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Box of 80 blisters of 6 chewable breakable tablets
- Box of 80 blisters of 6 chewable breakable tablets
- Box of 80 blisters of 6 chewable breakable tablets
- Box of 80 blisters of 6 chewable breakable tablets
- Box of 80 blisters of 6 chewable breakable tablets
- Box of 80 blisters of 6 chewable breakable tablets
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V442251
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0225/005
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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