Veterinary Medicines

Quinoflox 100 mg/ml solution for use in drinking water, chicken and rabbits

Authorised
  • Enrofloxacin
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Product identification

Medicine name:
Quinoflox 100 mg/ml solution for use in drinking water, chicken and rabbits
Quinoflox Oplossing voor gebruik in drinkwater
Quinoflox Solution pour administration dans l'eau de boisson
Quinoflox Lösung zum Eingeben über das Trinkwasser
Active substance:
  • Enrofloxacin
Target species:
  • Chicken (broiler)
  • Chicken (chick, for replacement)
  • Chicken (pullet future breeder)
  • Rabbit
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Enrofloxacin
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral solution
Withdrawal period by route of administration:
  • Oral use
    • Chicken (broiler)
      • Meat and offal
        4
        day
    • Chicken (chick, for replacement)
      • Meat and offal
        4
        day
    • Chicken (pullet future breeder)
      • Meat and offal
        4
        day
    • Rabbit
      • Meat and offal
        2
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • 1 litre white high density polyethylene containers, provided with green screw seal cap of the same material, with an aluminium disk sealed by induction.
  • 4 X 5 litre white high density polyethylene containers, provided with green screw seal cap of the same material, with an aluminium disk sealed by induction
  • 12 X 1 litre white high density polyethylene containers, provided with green screw seal cap of the same material, with an aluminium disk sealed by induction
  • 5 litre white high density polyethylene containers, provided with green screw seal cap of the same material, with an aluminium disk sealed by induction

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:
  • Global Vet Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • S P Veterinaria S.A.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V400434
Date of authorisation status change:
Reference member state:
  • Portugal
Procedure number:
  • PT/V/0144/001
Concerned member states:
  • Belgium
  • France
  • Germany
  • Italy
  • Poland
  • Romania
  • United Kingdom (Northern Ireland)

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 20/04/2022
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French (PDF)
Published on: 20/04/2022
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German (PDF)
Published on: 20/04/2022
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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: 20/04/2022
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French (PDF)
Published on: 20/04/2022
Download
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