Veterinary Medicines

PROTECTIX 400 MG/2000 MG SPOT-ON SOLUTION FOR DOGS OVER 25 KG UP TO 40 KG

Authorised
  • Imidacloprid
  • Permethrin
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Product identification

Medicine name:
PROTECTIX 400 MG/2000 MG SPOT-ON SOLUTION FOR DOGS OVER 25 KG UP TO 40 KG
ProtecTix (400 mg + 2000 mg)pipetkę 4 ml Roztwór do nakrapiania
Active substance:
  • Imidacloprid
  • Permethrin
Target species:
  • Dog
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Imidacloprid
    400.00
    milligram(s)
    /
    1.00
    Pipette
  • Permethrin
    2000.00
    milligram(s)
    /
    1.00
    Pipette
Pharmaceutical form:
  • Spot-on solution
Withdrawal period by route of administration:
  • Cutaneous use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP53AC54
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Package description:
  • Pack containing 1 PET/PE/aluminium/surlyn sachet containing one white polypropylene unit dose pipette
  • Pack containing 2 PET/PE/aluminium/surlyn sachets each containing one white polypropylene unit dose pipette
  • Pack containing 3 PET/PE/aluminium/surlyn sachets each containing one white polypropylene unit dose pipette
  • Pack containing 4 PET/PE/aluminium/surlyn sachets each containing one white polypropylene unit dose pipette
  • Pack containing 6 PET/PE/aluminium/surlyn sachets each containing one white polypropylene unit dose pipette
  • Pack containing 12 PET/PE/aluminium/surlyn sachets each containing one white polypropylene unit dose pipette
  • Pack containing 24 PET/PE/aluminium/surlyn sachets each containing one white polypropylene unit dose pipette

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:
  • Beaphar B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Beaphar B.V.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 3427
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0433/004
Concerned member states:
  • Croatia
  • Cyprus
  • Czechia
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Malta
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 27/11/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 27/11/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 27/11/2025
Download
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