SULFADIMERAZINE QALIAN
SULFADIMERAZINE QALIAN
Authorised
- Sulfadimidine
Product identification
Medicine name:
SULFADIMERAZINE QALIAN
Active substance:
- Sulfadimidine
Target species:
-
Cattle
-
Pig
-
Sheep
-
Goat
-
Rabbit
-
Poultry
Route of administration:
-
Intramuscular use
-
Oral use
-
Intravenous use
-
Intraperitoneal use
Product details
Active substance and strength:
-
Sulfadimidine308.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal12day
-
Milk5day
-
-
Pig
-
Meat and offal12day
-
-
Sheep
-
Meat and offal12day
-
Milk5day
-
-
Goat
-
Meat and offal12day
-
Milk5day
-
-
-
Oral use
-
Cattle
-
Meat and offal12day
-
Milk5day
-
-
Pig
-
Meat and offal12day
-
-
Rabbit
-
Meat and offal12day
-
-
Sheep
-
Meat and offal12day
-
Milk5day
-
-
Goat
-
Meat and offal12day
-
Milk5day
-
-
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.
-
-
-
Intravenous use
-
Cattle
-
Meat and offal12day
-
Milk5day
-
-
Pig
-
Meat and offal12day
-
-
Sheep
-
Meat and offal12day
-
Milk5day
-
-
Goat
-
Meat and offal12day
-
Milk5day
-
-
-
Intraperitoneal use
-
Cattle
-
Meat and offal12day
-
Milk5day
-
-
Pig
-
Meat and offal12day
-
-
Sheep
-
Meat and offal12day
-
Milk5day
-
-
Goat
-
Meat and offal12day
-
Milk5day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EQ03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription except for some pack sizes
Authorisation status:
-
Valid
Authorised in:
-
France
Available 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:
- Huvepharma S.A.
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/3396800 3/1990
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: 5/12/2022
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: 15/10/2025