KESIUM 400 MG / 100 MG CHEWABLE TABLETS FOR DOGS
KESIUM 400 MG / 100 MG CHEWABLE TABLETS FOR DOGS
Authorised
This information is not available for this product.
Product identification
Medicine name:
KESIUM 400 MG / 100 MG CHEWABLE TABLETS FOR DOGS
Kesium 400 mg/100 mg Tuggtablett
Active substance:
This information is not available for this product.
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
This information is not available for this product.
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:
-
Sweden
Package description:
- Box of 1 blister of 6 chewable breakable tablets
- Box of 2 blisters of 6 chewable breakable tablets
- Box of 4 blisters of 6 chewable breakable tablets
- Box of 6 blisters of 6 chewable breakable tablets
- Box of 8 blisters of 6 chewable breakable tablets
- Box of 10 blisters of 6 chewable breakable tablets
- Box of 12 blisters of 6 chewable breakable tablets
- Box of 14 blisters of 6 chewable breakable tablets
- Box of 16 blisters of 6 chewable breakable tablets
- Box of 40 blisters of 6 chewable breakable tablets
- Box of 80 blisters of 6 chewable breakable tablets
- Box of 3 blisters of 4 chewable breakable tablets
- Box of 6 blisters of 4 chewable breakable tablets
- Box of 9 blisters of 4 chewable breakable tablets
- Box of 12 blisters of 4 chewable breakable tablets
- Box of 15 blisters of 4 chewable breakable tablets
- Box of 18 blisters of 4 chewable breakable tablets
- Box of 21 blisters of 4 chewable breakable tablets
- Box of 24 blisters of 4 chewable breakable tablets
- Box of 60 blisters of 4 chewable breakable tablets
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) 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:
- Swedish Medical Products Agency
Authorisation number:
- 44788
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0225/004
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
This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 20/09/2023
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 22/09/2023
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