SYNULOX RTU 140 mg/38,5 mg suspenzija za injiciranje
SYNULOX RTU 140 mg/38,5 mg suspenzija za injiciranje
Authorised
- Clavulanic acid
- Amoxicillin
Product identification
Medicine name:
SYNULOX RTU 140 mg/38,5 mg suspenzija za injiciranje
Active substance:
- Clavulanic acid
- Amoxicillin
Target species:
-
Cattle
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Clavulanic acid38.50/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 offal56dayMeso in organi goveda: 56 dni
-
Milk60hourMleko ni primerno za prehrano ljudi do 60 ur po uporabi zdravila.
-
-
Pig
-
Meat and offal20dayMeso in organi prašičev: 20 dni
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Available in:
-
Slovenia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0325/002
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.
Slovenian (PDF)
Published on: 2/02/2024
Package Leaflet
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in another language below.
Slovenian (PDF)
Published on: 2/02/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 2/02/2024