Veterinary Medicines

Comforion vet 100 mg/ml solution for injection for horse, cattle and swine

Authorised
  • Ketoprofen
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Product identification

Medicine name:
Comforion vet 100 mg/ml solution for injection for horse, cattle and swine
Comforion vet, 100 mg/mL, otopina za injekciju, za konje, goveda i svinje
Active substance:
  • Ketoprofen
Target species:
  • Horse
  • Cattle
  • Pig
Route of administration:
  • Intravenous use
  • Intramuscular 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:
  • Intravenous use
    • Horse
      • Meat and offal
        4
        day
      • Milk
        0
        hour
    • Cattle
      • Meat and offal
        4
        day
      • Milk
        0
        hour
  • Intramuscular use
    • Cattle
      • Meat and offal
        4
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        4
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AE03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Croatia
Package description:
  • 10 x 100 ml amber glass vial type II with bromobutyl rubber stopper type I and aluminium cap.
  • 10 x 50 ml amber glass vial type II with bromobutyl rubber stopper type I and aluminium cap.
  • 100 ml amber glass vial type II with bromobutyl rubber stopper type I and aluminium cap.
  • 50 ml amber glass vial type II with bromobutyl rubber stopper type I and aluminium cap.

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:
  • Orion Corporation
Marketing authorisation date:
Manufacturing sites for batch release:
  • Orion Corporation
  • Vetviva Richter GmbH
Responsible authority:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/23-01/863
Date of authorisation status change:
Reference member state:
  • Finland
Procedure number:
  • FI/V/0101/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Croatia
  • Czechia
  • Estonia
  • France
  • Hungary
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Romania
  • Slovakia
  • Slovenia
  • Sweden

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Croatian (PDF)
Published on: 11/06/2024
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