Veterinary Medicines

ALGENAMIC 40 mg/ml solution for injection

Authorised
  • Tolfenamic acid
Download as PDF

Product identification

Medicine name:
ALGENAMIC 40 mg/ml solution for injection
ALGENAMIC 40 mg/ml
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
    • Pig
      • Meat and offal
        16
        day
    • Dog
    • Cattle
      • Milk
        no withdrawal period
  • Intravenous use
    • Cattle
      • Meat and offal
        no withdrawal period
    • Cattle
      • Milk
        no withdrawal period
  • Subcutaneous use
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QM01AG02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
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:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 402749.00.00
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
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."