Veterinary Medicines Information website

Dugnixon 50 mg/ml Solution for Injection for Cattle, Pigs and Horses

Authorised
  • Flunixin meglumine
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Product identification

Medicine name:
Dugnixon 50 mg/ml Solution for Injection for Cattle, Pigs and Horses
Active substance:
  • Flunixin meglumine
Target species:
  • Cattle
  • Pig
  • Horse
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Flunixin meglumine
    82.90
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        31
        day
      • Milk
        36
        hour
    • Pig
      • Meat and offal
        24
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        4
        day
      • Milk
        24
        hour
    • Horse
      • Meat and offal
        5
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AG90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
Package description:
  • 250 ml sterile and translucent polypropylene vial with pink butyl rubber cap, grey aluminium cap and Flip-Off seal.
  • 100 ml sterile and translucent polypropylene vial with grey butyl rubber cap, grey aluminium cap and Flip-Off seal.
  • 50 ml sterile and translucent polypropylene vial with grey butyl rubber cap, grey aluminium cap and Flip-Off seal.

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:
  • Global Vet Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Sp Quimica S.A.
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 36167/4005
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0469/001
Concerned member states:
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 8/06/2025
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Combined File of all Documents

English (PDF)
Published on: 8/06/2025
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