CLAVASEPTIN 500MG PALATABLE TABLETS FOR DOGS
CLAVASEPTIN 500MG PALATABLE TABLETS FOR DOGS
Authorised
- Amoxicillin trihydrate
- Potassium clavulanate
Product identification
Medicine name:
CLAVASEPTIN 500MG PALATABLE TABLETS FOR DOGS
Clavaseptin, 500mg, Tableta
Active substance:
- Amoxicillin trihydrate
- Potassium clavulanate
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate459.11milligram(s)1.00Tablet
-
Potassium clavulanate119.10milligram(s)1.00Tablet
Pharmaceutical form:
-
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:
-
Czechia
Package description:
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Vetoquinol s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetoquinol S.A.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/049/11-C
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0407/003
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Denmark
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 12/03/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 12/03/2025
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