Veterinary Medicines

Ketofen 100 mg/ml Solution for Injection

Authorised
  • Ketoprofen
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Product identification

Medicine name:
Ketofen 100 mg/ml Solution for Injection
Active substance:
  • Ketoprofen
Target species:
  • Cattle
  • Horse
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Ketoprofen
    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
        4
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        1
        day
    • Horse
      • Meat and offal
        1
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AE03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • 250 mL type II brown glass vial with chlorobutyl stopper or 250 mL amber multilayer plastic (Polypropylene/Adhesive/ Ethylene vinyl alcohol layer/ Adhesive/ polypropylene) vial with bromobutyl stopper.Cardboard box of 1 vial.
  • 100 mL type II brown glass vial with chlorobutyl stopper or 100 mL amber multilayer plastic (Polypropylene/Adhesive/ Ethylene vinyl alcohol layer/ Adhesive/ polypropylene) vial with bromobutyl stopper.Cardboard box of 1 vial.
  • 50 mL type II brown glass vial with chlorobutyl stopper or 50 mL amber multilayer plastic (Polypropylene/Adhesive/ Ethylene vinyl alcohol layer/ Adhesive/ polypropylene) vial with bromobutyl stopper.Cardboard box of 1 vial.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
  • Merial
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10815/051/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 20/04/2025
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