Synulox RTU suspensija injekcijām liellopiem, cūkām, suņiem un kaķiem
Synulox RTU suspensija injekcijām liellopiem, cūkām, suņiem un kaķiem
Authorised
- Amoxicillin
- Potassium clavulanate
Product identification
Medicine name:
Synulox RTU suspensija injekcijām liellopiem, cūkām, suņiem un kaķiem
Active substance:
- Amoxicillin
- Potassium clavulanate
Target species:
-
Pig
-
Dog
-
Cat
-
Cattle
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Amoxicillin140.00milligram(s)1.00millilitre(s)
-
Potassium clavulanate35.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal31day
-
-
Dog
-
Cat
-
Cattle
-
Meat and offal42day
-
Milk60hour60 stundas (5 slaukšanas reizes, ja govs tiek slaukta divas reizes dienā)
-
-
-
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:
-
Latvia
Available in:
-
Latvia
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:
- Food And Veterinary Service
Authorisation number:
- V/NRP/02/1476
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
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 19/08/2024
How useful was this page?: