SYNULOX PALATABLE TABLETS 50 mg
SYNULOX PALATABLE TABLETS 50 mg
Authorised
- Potassium clavulanate
- Amoxicillin trihydrate
Product identification
Medicine name:
СИНУЛОКС ОВКУСЕНИ ТАБЛЕТИ 50 mg
SYNULOX PALATABLE TABLETS 50 mg
Active substance:
- Potassium clavulanate
- Amoxicillin trihydrate
Target species:
-
Dog
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Potassium clavulanate10.00/milligram(s)1.00Tablet
-
Amoxicillin trihydrate40.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-1611
Date of authorisation status change:
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.
Bulgarian (PDF)
Published on: 21/04/2022
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 21/04/2022
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