Veterinary Medicines

Amoxycilline 70 % Kela 700 mg/g Poeder voor toediening in het drinkwater/in de melk

Authorised
  • Amoxicillin trihydrate
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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 trihydrate
    817.70
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water/milk
Withdrawal period by route of administration:
  • In drinking water/milk use
    • Chicken
      • Meat and offal
        1
        day
      • Egg
        no withdrawal period
    • Pig
      • Meat and offal
        2
        day
    • Cattle (calf)
      • Meat and offal
        4
        day
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:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 11/02/2022
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French (PDF)
Published on: 11/02/2022
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German (PDF)
Published on: 11/02/2022
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 11/02/2022
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French (PDF)
Published on: 11/02/2022
Download
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