TRISULMIX POUDRE POUR SOLUTION BUVABLE
TRISULMIX POUDRE POUR SOLUTION BUVABLE
Authorised
- Sulfadimethoxine sodium
- Trimethoprim
Product identification
Medicine name:
TRISULMIX POUDRE POUR SOLUTION BUVABLE
Active substance:
- Sulfadimethoxine sodium
- Trimethoprim
Target species:
-
Fowl
-
Pig
-
Rabbit
-
Sheep (lamb)
-
Goat (kid)
-
Cattle (calf)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Sulfadimethoxine sodium200.00/milligram(s)1.00gram(s)
-
Trimethoprim40.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Fowl
-
Eggsno withdrawal periodEn l'absence d'un temps d'attente pour les œufs ne pas utiliser chez les volailles pondeuses productrices d'œufs de consommation (4 semaines avant le démarrage de la ponte et pendant celle-ci).
-
Meat and offal12day
-
-
Pig
-
Meat and offal12day
-
-
Rabbit
-
Meat and offal12day
-
-
Sheep (lamb)
-
Meat and offal12day
-
-
Goat (kid)
-
Meat and offal12day
-
-
Cattle (calf)
-
Meat and offal12day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Dopharma France
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma France
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/0086132 2/1992
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.
French (PDF)
Published on: 15/10/2025
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 14/03/2025