REFORDOG 40 mg/200 mg spot-on solution for dogs over 1.5 kg up to 4 kg
REFORDOG 40 mg/200 mg spot-on solution for dogs over 1.5 kg up to 4 kg
Authorised
- Imidacloprid
- Permethrin (40:60)
Product identification
Medicine name:
REFORDOG 40 mg/200 mg spot-on solution for dogs over 1.5 kg up to 4 kg
Refordog 40 mg/200 mg solution pour spot-on pour chiens de plus de 1,5 kg à 4 kg
Refordog 40 mg/200 mg spot-on oplossing voor honden vanaf 1,5 kg tot 4 kg
Refordog 40 mg/200 mg Lösung zum Auftropfen für Hunde über 1,5 kg bis 4 kg
Active substance:
- Imidacloprid
- Permethrin (40:60)
Target species:
-
Dog
Route of administration:
-
Spot-on use
Product details
Active substance and strength:
-
Imidacloprid40.00/milligram(s)1.00Pipette
-
Permethrin (40:60)200.00/milligram(s)1.00Pipette
Pharmaceutical form:
-
Spot-on solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AC54
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Cardboard box containing 1 pipette of 0.4 ml with pouch
- Cardboard box containing 2 pipettes of 0.4 ml with pouch
- Cardboard box containing 3 pipettes of 0.4 ml with pouch
- Cardboard box containing 4 pipettes of 0.4 ml with pouch
- Cardboard box containing 6 pipettes of 0.4 ml with pouch
- Cardboard box containing 24 pipettes of 0.4 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:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V663996
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0666/001
Concerned member states:
-
Austria
-
Belgium
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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Combined File of all Documents
English (PDF)
Download Published on: 30/11/2025