Veterinary Medicines

MARFLOQUIN 100 MG/ML SOLUTION FOR INJECTION FOR BOVINES AND PIGS (SOWS)

Authorised
  • Marbofloxacin
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Product identification

Medicine name:
MARFLOQUIN 100 MG/ML SOLUTION FOR INJECTION FOR BOVINES AND PIGS (SOWS)
Quiflox, 100mg/ml, Injekční roztok
Active substance:
  • Marbofloxacin
Target species:
  • Cattle
  • Pig (sow)
Route of administration:
  • Intramuscular use
  • Subcutaneous use
  • Intravenous use

Product details

Active substance and strength:
  • Marbofloxacin
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        36
        hour
      • Meat and offal
        6
        day
      • Milk
        72
        hour
      • Meat and offal
        3
        day
    • Pig (sow)
      • Meat and offal
        4
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        6
        day
      • Milk
        36
        hour
  • Intravenous use
    • Cattle
      • Meat and offal
        6
        day
      • Milk
        36
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MA93
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Available in:
  • Czechia
Package description:
  • Box of one 50 ml solution bottle for injection
  • Box of one 250 ml solution bottle for injection
  • Box of one 100 ml solution bottle for injection

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:
  • KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
  • KRKA tovarna zdravil d.d. Novo mesto
  • Virbac
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/077/11-C
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0223/002
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Portugal
  • Slovakia
  • Spain

Documents

Summary of Product Characteristics

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Czech (PDF)
Published on: 12/12/2025
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Package Leaflet

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Czech (PDF)
Published on: 12/12/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 12/12/2025
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