Clavucill 200 mg + 50 mg 200 mg - 50 mg Tablet
Clavucill 200 mg + 50 mg 200 mg - 50 mg Tablet
Authorised
- Amoxicillin trihydrate
- POTASSIUM CLAVULANATE DILUTED WITH CELLULOSE, MICROCRYSTALLINE (1:1)
Product identification
Medicine name:
Clavucill 200 mg/50 mg Tablett
Clavucill 200 mg + 50 mg 200 mg - 50 mg Tablet
Active substance:
- Amoxicillin trihydrate
- POTASSIUM CLAVULANATE DILUTED WITH CELLULOSE, MICROCRYSTALLINE (1:1)
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate229.55milligram(s)1.00Tablet
-
POTASSIUM CLAVULANATE DILUTED WITH CELLULOSE, MICROCRYSTALLINE (1:1)125.10milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Sweden
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
- V.M.D.
Responsible authority:
- Swedish Medical Products Agency
Authorisation number:
- 46021
Date of authorisation status change:
Reference member state:
-
Belgium
Procedure number:
- BE/V/0024/002
Concerned member states:
-
Denmark
-
France
-
Germany
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Spain
-
Sweden
Generic of:
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.
Swedish (PDF)
Published on: 26/04/2022
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 26/04/2022
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