SURRICOXX 400 MG/ML SOLUTION FOR USE IN DRINKING WATER FOR CHICKENS, TURKEYS, DUCKS, AND GUINEA FOWLS
SURRICOXX 400 MG/ML SOLUTION FOR USE IN DRINKING WATER FOR CHICKENS, TURKEYS, DUCKS, AND GUINEA FOWLS
Authorised
- Amprolium hydrochloride
Product identification
Medicine name:
SURRICOXX 400 MG/ML SOLUTION FOR USE IN DRINKING WATER FOR CHICKENS, TURKEYS, DUCKS, AND GUINEA FOWLS
SURRICOXX 400 mg/ml roztok na použitie v pitnej vode pre kurčatá, morky, kačky a perličky
Active substance:
- Amprolium hydrochloride
Target species:
-
Turkey
-
Guinea fowl
-
Duck
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Amprolium hydrochloride452.40/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Turkey
-
Meat and offal0day
-
Eggs0day
-
-
Guinea fowl
-
Meat and offal0day
-
Eggs0day
-
-
Duck
-
Meat and offal0day
-
Eggs0day
-
-
Chicken
-
Meat and offal0day
-
Eggs0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP51AX09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratoires Biove
- V.M.D.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/003/DC/21-S
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0422/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Czechia
-
Estonia
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 10/08/2023