Veterinary Medicines

Doxylin 100%, powder for use in drinking water/milk for calves and pigs

Authorised
  • Doxycycline hyclate
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Product identification

Medicine name:
Doxylin 100%, powder for use in drinking water/milk for calves and pigs
Doxylin 100% 1000 mg/g Poeder voor toediening in het drinkwater/in de melk
Doxylin 100% 1000 mg/g Poudre pour administration dans le lait ou l'eau de boisson
Doxylin 100% 1000 mg/g Pulver zum Eingeben über das Trinkwasser/die Milch
Active substance:
  • Doxycycline hyclate
Target species:
  • Cattle (calf)
  • Pig
Route of administration:
  • In drinking water/milk use

Product details

Active substance and strength:
  • Doxycycline hyclate
    1000.00
    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
    • Cattle (calf)
      • Meat and offal
        14
        day
    • Pig
      • Meat and offal
        8
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • White polypropylene container (bucket) of 5 kg, covered with a polypropylene closure.
  • White polypropylene container (bucket) of 2 kg, covered with a polypropylene closure.
  • White polypropylene container of 100 grams, covered with a low-density polyethylene closure.
  • White polypropylene container (bucket) of 1 kg, covered with a polypropylene closure.
  • White polypropylene container of 1 kg, covered with a low-density polyethylene closure.

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:
  • Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Dopharma B.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0184/001
Concerned member states:
  • Belgium
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Poland
  • Romania

Documents

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: 28/02/2026
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French (PDF)
Published on: 28/02/2026
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German (PDF)
Published on: 28/02/2026
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 28/02/2026
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French (PDF)
Published on: 28/02/2026
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German (PDF)
Published on: 28/02/2026
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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: 28/02/2026
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French (PDF)
Published on: 28/02/2026
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German (PDF)
Published on: 28/02/2026
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Combined File of all Documents

English (PDF)
Published on: 28/01/2026
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