Veterinary Medicines

ALGENAMIC 40 mg/ml solution for injection for cattle, pigs, dogs and cats

Authorised
  • Tolfenamic acid
Download as PDF

Product identification

Medicine name:
ALGENAMIC 40 mg/ml solution for injection for cattle, pigs, dogs and cats
ALGENAMIC 40 mg / ml ενέσιμο διάλυμα για βοοειδή, χοίρους, σκύλους και γάτες
Active substance:
  • Tolfenamic acid
Target species:
  • Cattle
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Tolfenamic acid
    40.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        16
        day
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
  • Intravenous use
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AG02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Cyprus
Available in:
  • Cyprus
Package description:
  • Cardboard box with 15 glass vials of 250 ml
  • Cardboard box with 10 glass vials of 100 ml
  • Cardboard box with 5 glass vial of 20 ml
  • Cardboard box with 1 glass vial of 250 ml
  • Cardboard box with 1 glass vial of 100 ml
  • Cardboard box with 1 glass vial of 20 ml

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:
  • Vetpharma Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Mevet S.A.
Responsible authority:
  • Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
  • CY00847V
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0382/001
Concerned member states:
  • Austria
  • Belgium
  • Croatia
  • Cyprus
  • France
  • Germany
  • Greece
  • Italy
  • Poland
  • Portugal
  • Romania

Documents

Summary of Product Characteristics

English (PDF)
Published on: 22/12/2023
Download

Package Leaflet

English (PDF)
Published on: 27/06/2024
Download

Labelling

English (PDF)
Published on: 27/06/2024
Download

Combined File of all Documents

English (PDF)
Published on: 24/07/2025
Download
Greek (PDF)
Published on: 1/07/2025
Download