Rhemox 1000, 1000 mg/g Powder for Use in Drinking Water for Chickens, Ducks, Turkeys
Rhemox 1000, 1000 mg/g Powder for Use in Drinking Water for Chickens, Ducks, Turkeys
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Rhemox 1000, 1000 mg/g Powder for Use in Drinking Water for Chickens, Ducks, Turkeys
Rhemox Forte 1000 mg/g Proszek do podania w wodzie do picia
Active substance:
- Amoxicillin trihydrate
Target species:
-
Turkey
-
Duck
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Amoxicillin trihydrate1000.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Turkey
-
Meat and offal5day
-
Eggsno withdrawal periodEggs: Not authorised for use in laying birds producing eggs for human consumption. Do not use within 3 weeks of onset of the laying period.
-
- Duck
-
Meat and offal9day
-
Eggsno withdrawal periodEggs: Not authorised for use in laying birds producing eggs for human consumption. Do not use within 3 weeks of onset of the laying period.
-
- Chicken
-
Meat and offal1day
-
Eggsno withdrawal periodEggs: Not authorised for use in laying birds producing eggs for human consumption. Do not use within 3 weeks of onset of the laying period.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Available in:
-
Poland
Package description:
- sachet of 5 kg
- sachet of 1 kg
- sachet of 500 g
- sachet of 200 g
- sachet of 100 g
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Livisto Int'l S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Animedica GmbH
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2686
Reference member state:
-
Spain
Procedure number:
- ES/V/0331/001
Concerned member states:
-
Austria
-
Belgium
-
Germany
-
Greece
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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