SYNULOX RTU, injekcinė suspensija galvijams, kiaulėms, šunims ir katėms
SYNULOX RTU, injekcinė suspensija galvijams, kiaulėms, šunims ir katėms
Authorised
- Clavulanic acid
- Amoxicillin
Product identification
Medicine name:
SYNULOX RTU, injekcinė suspensija galvijams, kiaulėms, šunims ir katėms
Active substance:
- Clavulanic acid
- Amoxicillin
Target species:
-
Dog
-
Cat
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Clavulanic acid35.00/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 offal, milk42daypienui – 60 val. (5 melžimai, jei melžiama 2 kartus per parą)
-
-
Pig
-
Meat and offal31day
-
-
-
Subcutaneous use
-
Dog
-
Not applicable0day
-
-
Cat
-
Not applicable0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/01/1227/001-002
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
This document does not exist in this language (English). You can find it
in another language below.
Lithuanian (PDF)
Published on: 19/01/2023