Veterinary Medicine Information website

Marbocyl 20 mg/ml Solution for Injection

Authorised
  • Marbofloxacin
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Product identification

Medicine name:
Marbocyl 20 mg/ml Solution for Injection
Active substance:
  • Marbofloxacin
Target species:
  • Cattle
  • Pig
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Marbofloxacin
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        4
        day
    • Pig
      • Meat and offal
        2
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        4
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        4
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MA93
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • Marbocyl 2% injection is packaged in amber type II glass vial of 10 ml.The vial is closed with a chlorobutyl rubber stopper and oversealed with aluminium cap.Each vial is packaged in a cardboard box.
  • Marbocyl 2% injection is packaged in amber type II glass vial of 20 ml.The vial is closed with a chlorobutyl rubber stopper and oversealed with aluminium cap.Each vial is packaged in a cardboard box.
  • Marbocyl 2% injection is packaged in amber type II glass vial of 50 ml.The vial is closed with a chlorobutyl rubber stopper and oversealed with aluminium cap.Each vial is packaged in a cardboard box.
  • Marbocyl 2% injection is packaged in amber type II glass vial of 100 ml.The vial is closed with a chlorobutyl rubber stopper and oversealed with aluminium cap.Each vial is packaged in a cardboard box.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Vetoquinol Ireland Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol S.A.
  • Vetoquinol Biowet Sp. z o.o.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10983/032/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 24/11/2024
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