Veterinary Medicines

Quinoflox 100 mg/ml solution for injection for cattle and pigs

Authorised
  • Enrofloxacin
Download as PDF

Product identification

Medicine name:
Quinoflox, 100 mg/mL, otopina za injekciju, za goveda i svinje
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:
  • Croatia
Package description:
  • Amber polypropylene vial of 250 ml provided with a pink (250 ml) 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 50 ml provided with a grey 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:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/23-01/332
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

This document does not exist in this language (English). You can find it in another language below.
Croatian (PDF)
Published on: 9/10/2023
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."