Synuclav 200 mg / 50 mg Tablets for Dogs
Synuclav 200 mg / 50 mg Tablets for Dogs
Authorised
- Potassium clavulanate
- Amoxicillin trihydrate
Product identification
Medicine name:
Synuclav 200 mg / 50 mg Tablets for Dogs
Active substance:
- Potassium clavulanate
- Amoxicillin trihydrate
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Potassium clavulanate59.50/milligram(s)1.00Tablet
-
Amoxicillin trihydrate229.50/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:
-
France
Available in:
-
France
Package description:
- box containing 20 tablets (4 blister)
- box containing 50 tablets (10 blister)
- box containing 250 tablets (50 blister)
- bottle containing 100 tablets
- bottle containing 250 tablets
- box containing 100 tablets (20 blister)
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:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Laboratories (Ireland) Limited
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/1889296 5/2004
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0349/002
Concerned member states:
-
Belgium
-
France
-
Iceland
-
Italy
-
Portugal
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
