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Powdox Doxycycline 500 mg/g Powder for Use in Drinking Water for Pigs, Chickens and Turkeys

Authorised
  • Doxycycline hyclate
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Product identification

Medicine name:
Powdox Doxycycline 500 mg/g Powder for Use in Drinking Water for Pigs, Chickens and Turkeys
Active substance:
  • Doxycycline hyclate
Target species:
  • Chicken (for reproduction)
  • Chicken (broiler)
  • Pig (for fattening)
  • Turkey (for reproduction)
  • Turkey (for meat production)
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Doxycycline hyclate
    580.00
    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 (for reproduction)
      • Meat and offal
        5
        day
      • Eggs
        no withdrawal period
    • Chicken (broiler)
      • Meat and offal
        5
        day
      • Eggs
        no withdrawal period
    • Pig (for fattening)
      • Meat and offal
        4
        day
    • Turkey (for reproduction)
      • Meat and offal
        12
        day
      • Eggs
        no withdrawal period
    • Turkey (for meat production)
      • Meat and offal
        12
        day
      • Eggs
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
Available in:
  • United Kingdom (Northern Ireland)
Package description:
  • bag of 1 kg
  • bag of 200 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:
  • Vetpharma Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Karizoo S.A.
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 32509/4009
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0177/001
Concerned member states:
  • Austria
  • Bulgaria
  • Denmark
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Poland
  • Portugal
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 1/02/2024
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Package Leaflet

English (PDF)
Published on: 1/02/2024
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Labelling

English (PDF)
Published on: 1/02/2024
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Combined File of all Documents

English (PDF)
Published on: 24/07/2025
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