SYNULOX RTU ενέσιμο εναιώρημα για βοοειδή, χοίρους, σκύλους και γάτες
SYNULOX RTU ενέσιμο εναιώρημα για βοοειδή, χοίρους, σκύλους και γάτες
Authorised
- Potassium clavulanate
- Amoxicillin
Product identification
Medicine name:
SYNULOX RTU ενέσιμο εναιώρημα για βοοειδή, χοίρους, σκύλους και γάτες
Active substance:
- Potassium clavulanate
- Amoxicillin
Target species:
-
Cattle
-
Pig
-
Cat
-
Dog
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Potassium clavulanate35.00/milligram(s)1.00millilitre(s)
-
Amoxicillin140.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal42day
-
Milk60hour
-
-
Pig
-
Meat and offal26day
-
-
Cat
-
Not applicableno withdrawal period
-
-
Dog
-
Not applicableno withdrawal period
-
-
-
Subcutaneous use
-
Cat
-
Not applicableno withdrawal period
-
-
Dog
-
Not applicableno withdrawal period
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Available in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Zoetis Hellas S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- HAUPT PHARMA LATINA
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 31804/09-04-2021/K-0077403
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet