Suramox 500 mg/g pulveris šķīduma iekšķīgai lietošanai pagatavošanai cūkām
Suramox 500 mg/g pulveris šķīduma iekšķīgai lietošanai pagatavošanai cūkām
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Suramox 500 mg/g pulveris šķīduma iekšķīgai lietošanai pagatavošanai cūkām
Active substance:
- Amoxicillin trihydrate
Target species:
-
Pig
Route of administration:
-
In-feed use
-
In drinking water 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-feed use
-
Pig
-
Meat and offal14day
-
-
-
In drinking water use
-
Pig
-
Meat and offal14day
-
-
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:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/08/1716
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: 8/04/2025