Citramox 1000 mg/g powder for use in drinking water for chickens, ducks, turkeys and pigs
Citramox 1000 mg/g powder for use in drinking water for chickens, ducks, turkeys and pigs
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Citramox 1000 mg/g powder for use in drinking water for chickens, ducks, turkeys and pigs
Citramox 1000 mg/g κόνις για χορήγηση με πόσιμο νερό για όρνιθες, ινδόρνιθες, πάπιες και χοίρους
Active substance:
- Amoxicillin trihydrate
Target species:
-
Turkey
-
Chicken
-
Duck
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate1000.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
Oral use
-
Turkey
-
Meat and offal5day
-
-
Chicken
-
Meat and offal1day
-
-
Duck
-
Meat and offal9day
-
-
Pig
-
Meat and offal2day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Package description:
- Thermosealed bags made of polyester, aluminium and polyethylene complex.Pack sizes: 20 x 200 g
- Thermosealed bags made of polyester, aluminium and polyethylene complex.Pack sizes: 1 kg bag
- Thermosealed bags made of polyester, aluminium and polyethylene complex.Pack sizes: 500 g bag
- Thermosealed bags made of polyester, aluminium and polyethylene complex.Pack sizes: 200 g bag
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:
- Laboratorios Karizoo S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Karizoo S.A.
Responsible authority:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
- CY00777V
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0353/001
Concerned member states:
-
Cyprus
-
Czechia
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet