Veterinary Medicines

QUINOLCEN 100 mg/ml Injection

Authorised
  • Enrofloxacin
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Product identification

Medicine name:
QUINOLCEN 100 mg/ml Injection
Colmyc 100mg/ml ενέσιμο διάλυμα για βοοειδή, χοίρους, πρόβατα και αίγες
Active substance:
  • Enrofloxacin
Target species:
  • Cattle
  • Sheep
  • Goat
  • Pig
Route of administration:
  • Subcutaneous use
  • Intravenous use
  • Intramuscular 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:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        no withdrawal period
    • Sheep
      • Meat and offal
        4
        day
    • Goat
      • Meat and offal
        6
        day
    • Cattle
      • Milk
        no withdrawal period
    • Sheep
      • Milk
        3
        day
    • Goat
      • Milk
        4
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        no withdrawal period
    • Cattle
      • Milk
        no withdrawal period
  • Intramuscular use
    • Pig
      • Meat and offal
        13
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Greece
Package description:
  • box containing 1 vial of 250 ml
  • box containing 1 vial of 100 ml
  • box containing 1 vial of 50 ml

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:
  • S P Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • S P Veterinaria S.A.
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 6375/01-02-2016/K-0185001
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0150/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Greece
  • Hungary
  • Italy
  • Luxembourg
  • Poland
  • Portugal
  • Romania

Documents

Summary of Product Characteristics

English (PDF)
Published on: 5/04/2023
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Greek (PDF)
Published on: 5/09/2023
Updated on: 7/09/2023
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Package Leaflet

English (PDF)
Published on: 5/04/2023
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Combined File of all Documents

English (PDF)
Published on: 24/07/2025
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