VETRIMOXIN 500mg/g, pulveris iekšķīgi lietojama šķīduma pagatavošanai
VETRIMOXIN 500mg/g, pulveris iekšķīgi lietojama šķīduma pagatavošanai
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
VETRIMOXIN 500mg/g, pulveris iekšķīgi lietojama šķīduma pagatavošanai
Active substance:
- Amoxicillin trihydrate
Target species:
-
Poultry
-
Pig
-
Cattle (suckling calf)
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Amoxicillin trihydrate500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Poultry
-
Meat and offal3dayNav reģistrēts lietošanai putniem, no kuriem iegūst olas lietošanai pārtikā.
-
-
Pig
-
Meat and offal7day
-
-
Cattle (suckling calf)
-
Meat and offal1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/03/1588
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.
Latvian (PDF)
Published on: 22/03/2024
Package Leaflet
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in another language below.
Latvian (PDF)
Published on: 22/03/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 22/03/2024