Veterinary Medicines

Fyperix 134 mg spot-on solution for dogs

Authorised
  • Fipronil
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Product identification

Medicine name:
Fyperix 134 mg spot-on solution for dogs
FYPERIX 134 MG SOLUTION SPOT-ON POUR CHIENS
Active substance:
  • Fipronil
Target species:
  • Dog
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Fipronil
    134.00
    milligram(s)
    /
    0.67
    millilitre(s)
Pharmaceutical form:
  • Spot-on solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP53AX15
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Available in:
  • France
Package description:
  • (ID6) 40.2 millilitre(s): Box (Cardboard) with 30 Beutel (PolyEthylene TerePhthalate; Aluminium; Low Density PolyEthylene) each with 1 Pipette (PolyPropylene) with 1.34 millilitre(s)
  • (ID5) 26.8 millilitre(s): Box (Cardboard) with 20 Beutel (PolyEthylene TerePhthalate; Aluminium; Low Density PolyEthylene) each with 1 Pipette (PolyPropylene) with 1.34 millilitre(s)
  • (ID4) 13.4 millilitre(s): Box (Cardboard) with 10 Beutel (PolyEthylene TerePhthalate; Aluminium; Low Density PolyEthylene) each with 1 Pipette (PolyPropylene) with 1.34 millilitre(s)
  • (ID3) 8.04 millilitre(s): Box (Cardboard) with 6 Beutel (PolyEthylene TerePhthalate; Aluminium; Low Density PolyEthylene) each with 1 Pipette (PolyPropylene) with 1.34 millilitre(s)
  • (ID2) 4.02 millilitre(s): Box (Cardboard) with 3 Beutel (PolyEthylene TerePhthalate; Aluminium; Low Density PolyEthylene) each with 1 Pipette (PolyPropylene) with 1.34 millilitre(s)
  • (ID1) 1.34 millilitre(s): Box (Cardboard) with Beutel (PolyEthylene TerePhthalate; Aluminium; Low Density PolyEthylene) with 1 Pipette (PolyPropylene) with 1.34 millilitre(s)

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:
  • KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
  • KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/8246339 3/2012
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0190/003
Concerned member states:
  • Finland
  • France
  • Italy
  • Portugal
  • Spain

Documents

Summary of Product Characteristics

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French (PDF)
Published on: 7/04/2022
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