Veterinary Medicines

REMUVET 40 MG/200 MG SPOT-ON SOLUTION FOR DOGS UP TO 4 KG

Authorised
  • Imidacloprid
  • Permethrin
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Product identification

Medicine name:
REMUVET 40 MG/200 MG SPOT-ON SOLUTION FOR DOGS UP TO 4 KG
REMUVET 40 mg/200 mg soluzione spot-on per cani di peso fino a 4 kg
Active substance:
  • Imidacloprid
  • Permethrin
Target species:
  • Dog
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Imidacloprid
    40.00
    milligram(s)
    /
    1.00
    Pipette
  • Permethrin
    200.00
    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 not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:
  • Pack containing 24 PET/PE/aluminium/surlyn sachets each containing one white polyproylene unit dose pipette
  • Pack containing 12 PET/PE/aluminium/surlyn sachets each containing one white polyproylene unit dose pipette
  • Pack containing 6 PET/PE/aluminium/surlyn sachets each containing one white polyproylene unit dose pipette
  • Pack containing 4 PET/PE/aluminium/surlyn sachets each containing one white polyproylene unit dose pipette
  • Pack containing 3 PET/PE/aluminium/surlyn sachets each containing one white polyproylene unit dose pipette
  • Pack containing 2 PET/PE/aluminium/surlyn sachets each containing one white polyproylene unit dose pipette
  • Pack containing 1 PET/PE/aluminium/surlyn sachet containing one white polyproylene 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:
  • Ministry Of Health
Authorisation number:
  • 105644
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0440/001
Concerned member states:
  • Italy
  • Portugal
  • Spain

Documents

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Italian (PDF)
Published on: 9/04/2024
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