PULSIX 250 mg/1250 mg spot-on solution for dogs over 10 kg up to 25 kg
PULSIX 250 mg/1250 mg spot-on solution for dogs over 10 kg up to 25 kg
Authorised
- Imidacloprid
- Permethrin (40:60)
Product identification
Medicine name:
PULSIX 250 mg/1250 mg spot-on solution for dogs over 10 kg up to 25 kg
PULSIX 250 MG/1250 MG SOLUTION POUR SPOT-ON POUR CHIENS DE 10 KG A 25 KG
Active substance:
- Imidacloprid
- Permethrin (40:60)
Target species:
-
Dog
Route of administration:
-
Spot-on use
Product details
Active substance and strength:
-
Imidacloprid250.00milligram(s)1.00Pipette
-
Permethrin (40:60)1250.00milligram(s)1.00Pipette
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 2.5 ml without pouch
- Cardboard box containing 2 pipettes of 2.5 ml with pouch
- Cardboard box containing 2 pipettes of 2.5 ml without pouch
- Cardboard box containing 3 pipettes of 2.5 ml with pouch
- Cardboard box containing 3 pipettes of 2.5 ml without pouch
- Cardboard box containing 4 pipettes of 2.5 ml with pouch
- Cardboard box containing 4 pipettes of 2.5 ml without pouch
- Cardboard box containing 6 pipettes of 2.5 ml with pouch
- Cardboard box containing 6 pipettes of 2.5 ml without pouch
- Cardboard box containing 1 pipette of 2.5 ml with pouch
- Cardboard box containing 24 pipettes of 2.5 ml with pouch
- Cardboard box containing 24 pipettes of 2.5 ml without pouch
- Cardboard box containing 12 pipettes of 2.5 ml without pouch
- Cardboard box containing 12 pipettes of 2.5 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:
- Ab7 Sante
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/4138048 6/2024
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0667/003
Concerned member states:
-
France
-
Germany
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 20/10/2024
French (PDF)
Published on: 16/10/2024
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: 16/10/2024
ie-puar-mr-iev0667003-pulsix-250-mg1250-mg-spot-on-solution-for-dogs-ove-en.pdf
English (PDF)
Download Published on: 20/10/2024
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