Klavuxil 140 mg/mL + 35 mg/mL, suspenzija za injekciju, za goveda, pse i mačke
Klavuxil 140 mg/mL + 35 mg/mL, suspenzija za injekciju, za goveda, pse i mačke
Authorised
- Amoxicillin trihydrate
- Clavulanic acid
Product identification
Medicine name:
Klavuxil 140 mg/mL + 35 mg/mL, suspenzija za injekciju, za goveda, pse i mačke
Active substance:
- Amoxicillin trihydrate
- Clavulanic acid
Target species:
-
Cattle
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Amoxicillin trihydrate140.00milligram(s)1.00millilitre(s)
-
Clavulanic acid35.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal42day
-
Milk60hourMlijeko se ne smije koristiti za hranu 60 sati nakon liječenja tj. nakon 5. mužnje, ako se krave muze 2x na dan.
-
-
Subcutaneous use
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Croatia
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:
- Genera d.d.
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera d.d.
- Norbrook Laboratories Limited
Responsible authority:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
- UP/I-322-05/18-01/88
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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Croatian (PDF)
Published on: 14/02/2022
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