Veterinary Medicines

REFORDOG 600 mg/3000 mg spot-on solution for dogs over 40 kg up to 60 kg

Authorised
  • Imidacloprid
  • Permethrin (40:60)
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Product identification

Medicine name:
REFORDOG 600 mg/3000 mg spot-on solution for dogs over 40 kg up to 60 kg
REFORDOG 600 MG/3000 MG SOLUTION POUR SPOT-ON POUR CHIENS DE PLUS DE 40 KG A 60 KG
Active substance:
  • Imidacloprid
  • Permethrin (40:60)
Target species:
  • Dog
Route of administration:
  • Spot-on use

Product details

Active substance and strength:
  • Imidacloprid
    600.00
    milligram(s)
    /
    1.00
    Pipette
  • Permethrin (40:60)
    3000.00
    milligram(s)
    /
    1.00
    Pipette
Pharmaceutical form:
  • Spot-on solution
Withdrawal period by route of administration:
  • Spot-on use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP53AC54
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:
  • Cardboard box containing 1 pipette of 6.0 ml with pouch
  • Cardboard box containing 1 pipette of 6.0 ml without pouch
  • Cardboard box containing 2 pipettes of 6.0 ml without pouch
  • Cardboard box containing 2 pipettes of 6.0 ml with pouch
  • Cardboard box containing 3 pipettes of 6.0 ml with pouch
  • Cardboard box containing 3 pipettes of 6.0 ml without pouch
  • Cardboard box containing 4 pipettes of 6.0 ml without pouch
  • Cardboard box containing 4 pipettes of 6.0 ml with pouch
  • Cardboard box containing 6 pipettes of 6.0 ml with pouch
  • Cardboard box containing 6 pipettes of 6.0 ml without pouch
  • Cardboard box containing 24 pipettes of 6.0 ml without pouch
  • Cardboard box containing 24 pipettes of 6.0 ml with pouch

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Vetpharma Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • AB7 SANTE
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/7711657 0/2024
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0666/005
Concerned member states:
  • Austria
  • Belgium
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Netherlands
  • Poland
  • Portugal
  • Spain
  • 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.
French (PDF)
Published on: 25/03/2025
Download

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: 30/10/2024
Download
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