Synulox Ready-To-Use 140 mg/ml Suspensie voor injectie
Synulox Ready-To-Use 140 mg/ml Suspensie voor injectie
Authorised
- Clavulanic acid
- Amoxicillin trihydrate
Product identification
Medicine name:
Synulox Ready-To-Use 140 mg/ml Suspensie voor injectie
Active substance:
- Clavulanic acid
- Amoxicillin trihydrate
Target species:
-
Cat
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clavulanic acid35.00/milligram(s)1.00millilitre(s)
-
Amoxicillin trihydrate160.72/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:
-
Belgium
Package description:
- Synulox Ready-To-Use 12 x 50 ml Vial with Suspension for injection
- Synulox Ready-To-Use 12 x 20 ml Vial with Suspension for injection
- Synulox Ready-To-Use 12 x 10 ml Vial with Suspension for injection
- Synulox Ready-To-Use 1 x 100 ml Vial with Suspension for injection
- Synulox Ready-To-Use 1 x 50 ml Vial with Suspension for injection
- Synulox Ready-To-Use 1 x 20 ml Vial with Suspension for injection
- Synulox Ready-To-Use 1 x 10 ml Vial with 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:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V181614
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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Package Leaflet
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Labelling
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