Veterinary Medicines

Finadyne, 50 mg/ml, solution for injection

Authorised
  • Flunixin meglumine
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Product identification

Medicine name:
FINADYNE 50 MG/ML SOLUTION INJECTABLE POUR BOVINS, CHEVAUX ET PORCS
Finadyne, 50 mg/ml, solution for injection
Active substance:
  • Flunixin meglumine
Target species:
  • Cattle
  • Horse
  • Pig
Route of administration:
  • Intravenous use
  • Intramuscular use
  • Intramuscular use
  • Intramuscular use

Product details

Active substance and strength:
  • Flunixin meglumine
    83.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        4
        day
      • Milk
        24
        hour
    • Horse
      • Meat and offal
        5
        day
      • Milk
        no withdrawal period
  • Intramuscular use
    • Pig
      • Meat and offal
        24
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        31
        day
  • Intramuscular use
    • Cattle
      • Milk
        36
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AG90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:
  • 1 Cardboard box with 10 x 50 ml vial
  • 1 Cardboard box with 1 x 250 ml vial
  • 1 Cardboard box with 1 x 100 ml vial
  • 1 Cardboard box with 1 x 50 ml vial
  • 1 Cardboard box with 6 x 50 ml vial
  • 1 Cardboard box with 6 x 250 ml vial
  • 1 Cardboard box with 10 x 100 ml vial

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet
Marketing authorisation date:
Manufacturing sites for batch release:
  • Trirx Segre
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/0046543 8/1981
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 11/10/2024
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 15/10/2025
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Combined File of all Documents

English (PDF)
Published on: 5/06/2025
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