Synulox RTU 140/35 mg/ml Injektionssuspension für Rinder, Schweine (Ferkel, Mastschweine), Hunde und Katzen
Synulox RTU 140/35 mg/ml Injektionssuspension für Rinder, Schweine (Ferkel, Mastschweine), Hunde und Katzen
Authorised
- Amoxicillin trihydrate
- Potassium clavulanate
Product identification
Medicine name:
Synulox RTU 140/35 mg/ml Injektionssuspension für Rinder, Schweine (Ferkel, Mastschweine), Hunde und Katzen
Active substance:
- Amoxicillin trihydrate
- Potassium clavulanate
Target species:
-
Cattle
-
Dog
-
Cat
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Amoxicillin trihydrate161.00/milligram(s)1.00millilitre(s)
-
Potassium clavulanate41.65/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milk4day
-
Meat and offal14day
-
-
Pig
-
Meat and offal16day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
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 Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 400606.00.00
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Published on: 17/11/2025