Clavubactin 500/125 mg tablet
Clavubactin 500/125 mg tablet
Not authorised
- Amoxicillin
- Clavulanic acid
Product identification
Medicine name:
Clavubactin 500/125 mg tablet
Clavubactin 500 mg - 125 mg Tablet
Clavubactin 500 mg - 125 mg Comprimé
Clavubactin 500 mg - 125 mg Tablette
Active substance:
- Amoxicillin
- Clavulanic acid
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin500.00/milligram(s)1.00Tablet
-
Clavulanic acid125.00/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:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Aluminium/aluminium strips with 4 tablets, in a cardboard box containing 25 strips.
- Aluminium/aluminium strips with 2 tablets, in a cardboard box containing 5 strips.
- Aluminium/aluminium strips with 10 tablets, in a cardboard box containing 25 strips.
- Aluminium/aluminium strips with 10 tablets, in a cardboard box containing 10 strips.
- Aluminium/aluminium strips with 10 tablets, in a cardboard box containing 1 strip
- Cardboard box containing 10 separate cardboard boxes, each containing 5 Aluminium/aluminium strips with 2 tablets each.
- Aluminium/aluminium strips with 4 tablets, in a cardboard box containing 50 strips.
- Aluminium/aluminium strips with 4 tablets, in a cardboard box containing 5 strips.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Le Vet. B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Lelypharma B.V.
- Pharmachem Consulting ApS
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V261082
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0110/003
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.
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Labelling
This document does not exist in this language (English). You can find it
in another language below.
