Synulox Ready-To-Use, 140 mg/ml + 35 mg/ml, suspension injectable pour chiens et chats
Synulox Ready-To-Use, 140 mg/ml + 35 mg/ml, suspension injectable pour chiens et chats
Authorised
- Amoxicillin
- Clavulanic acid
Product identification
Medicine name:
Synulox Ready-To-Use, 140 mg/ml + 35 mg/ml, suspension injectable pour chiens et chats
Synulox Ready-To-Use 140 mg/ml Injektionssuspension
Active substance:
- Amoxicillin
- Clavulanic acid
Target species:
-
Dog
-
Cat
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Amoxicillin140.00/milligram(s)1.00millilitre(s)
-
Clavulanic acid35.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Luxembourg
Package description:
- Synulox Ready-To-Use 10 ml Vial Suspension for injection
- Synulox Ready-To-Use 20 ml Vial Suspension for injection
- Synulox Ready-To-Use 50 ml Vial Suspension for injection
- Synulox Ready-To-Use 100 ml Vial Suspension for injection
- Synulox Ready-To-Use 12 10 ml Vial Suspension for injection
- Synulox Ready-To-Use 12 20 ml Vial Suspension for injection
- Synulox Ready-To-Use 12 50 ml Vial Suspension for injection
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
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Ministry Of Health And Social Security
Authorisation number:
- V 087/97/04/0455
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
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in another language below.
French (PDF)
Published on: 16/03/2023