Veterinary Medicines

Tylosine 75 % Kela 750 mg/g Poeder voor gebruik in drinkwater

Authorised
  • Tylosin tartrate
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Product identification

Medicine name:
Tylosine 75 % Kela 750 mg/g Poeder voor gebruik in drinkwater
Tylosine 75 % Kela 750 mg/g Poudre pour administration dans l’eau de boisson
Tylosine 75 % Kela 750 mg/g Pulver zum Eingeben über das Trinkwasser
Active substance:
  • Tylosin tartrate
Target species:
  • Chicken
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Tylosin tartrate
    825.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Chicken
      • Meat and offal
        1
        day
      • Egg
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01FA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Tylosine 75 % Kela 1 Bag with 2000 g of Powder for use in drinking water
  • Tylosine 75 % Kela 1 Bag with 1333 g of Powder for use in drinking water
  • Tylosine 75 % Kela 1 Bag with 1000 g of Powder for use in drinking water
  • Tylosine 75 % Kela 1 Bag with 667 g of Powder for use in drinking water
  • Tylosine 75 % Kela 1 Bag with 500 g of Powder for use in drinking water
  • Tylosine 75 % Kela 1 Bag with 133 g of Powder for use in drinking water
  • Tylosine 75 % Kela 1 Bag with 100 g of Powder for use in drinking water

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-V216422
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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Package Leaflet

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Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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