File downloaded on 2026-04-20
Source URL: https://medicines.health.europa.eu/veterinary/en/600000046378
Authorised

Product identification

Medicine name:
Quinoflox 100 mg/ml solution for injection for cattle and pigs
Active substance:
  • Enrofloxacin
Target species:
  • Pig
  • Cattle
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Enrofloxacin
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        13
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        5
        day
      • Milk
        72
        hour
  • Subcutaneous use
    • Cattle
      • Meat and offal
        12
        day
      • Milk
        96
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Package description:
  • Amber polypropylene vial of 50 ml provided with a grey rubber-butyl stopper and aluminium seal with a green Flip-Off sealing.
  • Amber polypropylene vial of 100 ml provided with a grey rubber-butyl stopper and aluminium seal with a green Flip-Off sealing.
  • Amber polypropylene vial of 250 ml provided with a pink (250 ml) rubber-butyl stopper and aluminium seal with a green Flip-Off sealing.

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:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 2366
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0290/001
Concerned member states:
  • Bulgaria
  • Croatia
  • Poland
  • Portugal
  • Romania
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 16/01/2026
Download
Polish (PDF)
Published on: 12/06/2023
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 12/06/2023
Download

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 12/06/2023
Download