SULFALON
SULFALON
Authorised
- Sulfadimethoxine
Product identification
Medicine name:
SULFALON
Active substance:
- Sulfadimethoxine
Target species:
-
Cattle
-
Pig
-
Cat
-
Dog
-
Poultry
-
Horse
-
Horse (mare)
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Sulfadimethoxine200.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal10day
-
Milk5day
-
-
Pig
-
Meat and offal10day
-
-
Poultry
-
Meat and offal12day
-
Eggsno withdrawal periodEn l'absence de LMR pour les œufs, ne pas utiliser chez les espèces pondeuses productrices d'œufs de consommation, 4 semaines avant le démarrage de la ponte et pendant celle-ci
-
-
-
Intravenous use
-
Cattle
-
Meat and offal10day
-
Milk5day
-
-
Pig
-
Meat and offal10day
-
-
Horse (mare)
-
Milkno withdrawal periodEn l'absence de LMR pour le lait, ne pas utiliser chez les juments productrices de lait de consommation en lactation ou en période de tarissement ni chez les futures productrices de lait de consommation dans les 2 mois qui précèdent la mise-bas.
-
-
Poultry
-
Meat and offal12day
-
Eggsno withdrawal periodEn l'absence de LMR pour les oeufs, ne pas utiliser chez les espèces pondeuses productrices d'oeufs de consommation, 4 semaines avant le démarrage de la ponte et pendant celle-ci.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EQ09
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:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/9778988 8/1984
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: 4/04/2022
