Veterinary Medicines Information website

QUINOLCEN 100 mg/ml Injection

Not authorised
  • Enrofloxacin
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Product identification

Medicine name:
QUINOLCEN 100 mg/ml Injection
Active substance:
  • Enrofloxacin
Target species:
  • Cattle
  • Pig
  • Sheep
  • Goat
Route of administration:
  • Intramuscular 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
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        13
        day
    • Sheep
      • Meat and offal
        4
        day
      • Milk
        3
        day
    • Goat
      • Meat and offal
        6
        day
      • Milk
        4
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        13
        day
    • Sheep
      • Meat and offal
        4
        day
      • Milk
        3
        day
    • Goat
      • Meat and offal
        6
        day
      • Milk
        4
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Belgium
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:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V375654
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0150/001

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 22/03/2022
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Dutch (PDF)
Published on: 22/03/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 22/03/2022
Download
German (PDF)
Published on: 22/03/2022
Download
Dutch (PDF)
Published on: 22/03/2022
Download