Synulox Bolus 500 mg
Synulox Bolus 500 mg
Authorised
- Amoxicillin trihydrate
- Potassium clavulanate
Product identification
Medicine name:
Synulox Bolus 500 mg
Active substance:
- Amoxicillin trihydrate
- Potassium clavulanate
Target species:
-
Cattle
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate400.00/milligram(s)1.00Tablet
-
Potassium clavulanate100.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Coated tablet
Withdrawal period by route of administration:
-
Oral use
- Cattle
-
Meat and offal7day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Packs contain 20 boli, which are pink biconvex film coated tablets packed in heat sealed aluminium foil. Each bolus is individually heat sealed and contained in a strip of 10.
- Packs contain 500 boli, which are pink biconvex film coated tablets packed in heat sealed aluminium foil. Each bolus is individually heat sealed and contained in a strip of 10.
- Packs contain 100 boli, which are pink biconvex film coated tablets packed in heat sealed aluminium foil. Each bolus is individually heat sealed and contained in a strip of 10.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10387/072/001
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
English (PDF)
Download Published on: 3/05/2024
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