Veterinary Medicine Information website

Soludox 500 mg/g powder for use in drinking water for pigs and chickens

Authorised
  • Doxycycline hyclate
Download as PDF

Product identification

Medicine name:
Soludox 500 mg/g powder for use in drinking water for pigs and chickens
Active substance:
  • Doxycycline hyclate
Target species:
  • Chicken
  • Pig
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Doxycycline hyclate
    500.00
    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
        3
        day
      • Meat and offal
        9
        day
    • Pig
      • Meat and offal
        4
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovenia
Available in:
  • Slovenia
Package description:
  • The packs consists of one of the following laminates:Polyester / polyethylene / aluminium / polyethylene and an inner layer of polyethylene.Polyester / polyethylene / aluminium and an inner layer of ionomer (surlyn).Polyethylene terephtalic acid / aluminium / polyamide and an inner layerof polyethylene.Pack sizes of 100 g in a carton box.
  • The packs consists of one of the following laminates:Polyester / polyethylene / aluminium / polyethylene and an inner layer of polyethylene.Polyester / polyethylene / aluminium and an inner layer of ionomer (surlyn).Polyethylene terephtalic acid / aluminium / polyamide and an inner layerof polyethylene.Pack sizes of 250 g in a carton box.
  • The packs consists of one of the following laminates:Polyester / polyethylene / aluminium / polyethylene and an inner layer of polyethylene.Polyester / polyethylene / aluminium and an inner layer of ionomer (surlyn).Polyethylene terephtalic acid / aluminium / polyamide and an inner layerof polyethylene.Pack sizes of 500 g in a carton box.
  • The packs consists of one of the following laminates:Polyester / polyethylene / aluminium / polyethylene and an inner layer of polyethylene.Polyester / polyethylene / aluminium and an inner layer of ionomer (surlyn).Polyethylene terephtalic acid / aluminium / polyamide and an inner layerof polyethylene.Pack sizes of 1 kg in a carton box.
  • The packs consists of one of the following laminates:Polyester / polyethylene / aluminium / polyethylene and an inner layer of polyethylene.Polyester / polyethylene / aluminium and an inner layer of ionomer (surlyn).Polyethylene terephtalic acid / aluminium / polyamide and an inner layerof polyethylene.Pack sizes of 10x100 g in a carton box.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Responsible authority:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • MR/V/0600/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0477/001
Concerned member states:
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Italy
  • Malta
  • Romania
  • Slovakia
  • Slovenia
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 14/09/2025
Download
Slovenian (PDF)
Published on: 2/03/2022
Download

Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 2/03/2022
Download

Combined File of all Documents

English (PDF)
Published on: 14/09/2025
Download