Cylanic 250 mg + 62.5 mg tablets for dogs and cats
Cylanic 250 mg + 62.5 mg tablets for dogs and cats
Authorised
- Amoxicillin trihydrate
- Potassium clavulanate
Product identification
Medicine name:
Cylanic 250 mg + 62.5 mg tablets for dogs and cats
Cylanic 250 mg - 62.5 mg Tablet
Cylanic 250 mg - 62.5 mg Comprimé
Cylanic 250 mg - 62.5 mg Tablette
Active substance:
- Amoxicillin trihydrate
- Potassium clavulanate
Target species:
-
Dog
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate287.01/milligram(s)1.00Tablet
-
Potassium clavulanate74.45/milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- oPA/Alu/PVC - PVC/Alu heat sealed blister containing 10 tablets each.Package sizes:Cardboard box of 250 tablets.
- oPA/Alu/PVC - PVC/Alu heat sealed blister containing 10 tablets each.Package sizes:Cardboard box of 100 tablets.
- oPA/Alu/PVC - PVC/Alu heat sealed blister containing 10 tablets each.Package sizes:Cardboard box of 50 tablets.
- oPA/Alu/PVC - PVC/Alu heat sealed blister containing 10 tablets each.Package sizes:Cardboard box of 30 tablets.
- oPA/Alu/PVC - PVC/Alu heat sealed blister containing 10 tablets each.Package sizes:Cardboard box of 10 tablets.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Industrial Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Lelypharma B.V.
- aniMedica GmbH
- Industrial Veterinaria S.A.
- aniMedica Herstellungs GmbH
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V593431
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0582/002
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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in another language below.
Labelling
This document does not exist in this language (English). You can find it
in another language below.
ie-puar-mr-iev0582002-cylanic-250-mg--625-mg-tablets-for-dogs-and-cats-en.pdf
English (PDF)
Download Published on: 25/01/2026