Noroclav 50 mg Tablets for Dogs and Cats
Noroclav 50 mg Tablets for Dogs and Cats
Authorised
- Amoxicillin trihydrate
- Potassium clavulanate
Product identification
Medicine name:
Noroclav 50 mg Tablets for Dogs and Cats
Noroclav 50 mg 40 mg - 10 mg Tablet
Noroclav 50 mg 40 mg - 10 mg Comprimé
Noroclav 50 mg 40 mg - 10 mg Tablette
Active substance:
- Amoxicillin trihydrate
- Potassium clavulanate
Target species:
-
Dog
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate45.92/milligram(s)1.00Tablet
-
Potassium clavulanate11.91/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:
- The product is supplied in high-density polyethylene tubs with a polypropylene screw cap lid containing 100 tablets.
- The product is supplied in high-density polyethylene tubs with a polyethylene screw cap lid containing 500 tablets.
- The product is presented in packs containing 2 blister strips (aluminium-aluminium) each containing 10 tablets per strip
- The product is presented in packs containing 10 blister strips (aluminium-aluminium) each containing 10 tablets per strip
- The product is presented in packs containing 50 blister strips (aluminium-aluminium) each containing 10 tablets per strip
Additional information
Entitlement type:
-
Marketing Authorisation
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Manufacturing Limited
- Norbrook Laboratories Limited
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0546/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
France
-
Luxembourg
-
Netherlands
-
Norway
-
Portugal
-
Spain
-
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.
Combined File of all Documents
English (PDF)
Download Published on: 2/03/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
