Amoxycilline 70 % Kela 700 mg/g Poeder voor toediening in het drinkwater/in de melk
Amoxycilline 70 % Kela 700 mg/g Poeder voor toediening in het drinkwater/in de melk
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Amoxycilline 70 % Kela 700 mg/g Poeder voor toediening in het drinkwater/in de melk
Amoxycilline 70 % Kela 700 mg/g Poudre pour administration dans le lait ou l'eau de boisson
Amoxycilline 70 % Kela 700 mg/g Pulver zum Eingeben über das Trinkwasser/die Milch
Active substance:
- Amoxicillin trihydrate
Target species:
-
Chicken
-
Pig
-
Cattle (calf)
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Amoxicillin trihydrate817.70/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Chicken
-
Meat and offal1day
-
Eggno withdrawal periodNot for use in chickens producing eggs for human consumption
-
-
Pig
-
Meat and offal2day
-
-
Cattle (calf)
-
Meat and offal4day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Amoxycilline 70 % Kela 700 mg/g Powder for use in drinking water/milk Bag with 2000 g powder
- Amoxycilline 70 % Kela 700 mg/g Powder for use in drinking water/milk Bag with 1429 g powder
- Amoxycilline 70 % Kela 700 mg/g Powder for use in drinking water/milk Bag with 1000 g powder
- Amoxycilline 70 % Kela 700 mg/g Powder for use in drinking water/milk Bag with 714 g powder
- Amoxycilline 70 % Kela 700 mg/g Powder for use in drinking water/milk Bag with 500 g powder
- Amoxycilline 70 % Kela 700 mg/g Powder for use in drinking water/milk Bag with 143 g powder
- Amoxycilline 70 % Kela 700 mg/g Powder for use in drinking water/milk Bag with 100 g powder
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Kela Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V233764
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Summary of Product Characteristics
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Labelling
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