Veterinary Medicines

Rifen 100 mg/ml - Injektionslösung für Pferde, Rinder und Schweine

Authorised
  • Ketoprofen
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Product identification

Medicine name:
Rifen 100 mg/ml - Injektionslösung für Pferde, Rinder und Schweine
Rifen 100 mg/ml injektionsvæske, opløsning
Active substance:
  • Ketoprofen
Target species:
  • Cattle
  • Pig
  • 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
        3
        day
      • Milk
        0
        hour
    • Pig
      • Meat and offal
        4
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        1
        day
      • Milk
        0
        hour
    • 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:
  • Denmark
Available in:
  • Denmark
Package description:
  • 10 x 100 ml Amber glass vials type II, with bromobutyl rubber stopper type I and aluminium caps.
  • 10 x 50 ml Amber glass vials type II, with bromobutyl rubber stopper type I and aluminium caps.
  • 100 ml Amber glass vials type II, with bromobutyl rubber stopper type I and aluminium caps.
  • 50 ml Amber glass vials type II, with bromobutyl rubber stopper type I and aluminium caps.

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:
  • Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetviva Richter GmbH
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 50252
Date of authorisation status change:
Reference member state:
  • Austria
Procedure number:
  • AT/V/0002/001
Concerned member states:
  • Belgium
  • Czechia
  • Denmark
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Netherlands
  • Poland
  • Portugal
  • Slovakia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Danish (PDF)
Published on: 7/04/2025
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Combined File of all Documents

English (PDF)
Published on: 3/05/2023
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