Veterinary Medicine Information website

Eliminall 50 mg spot-on solution for cats

Not authorised
  • Fipronil

Product identification

Medicine name:
Eliminall 50 mg spot-on solution for cats
Active substance:
  • Fipronil
Target species:
  • Cat
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Fipronil
    50.00
    milligram(s)
    /
    0.50
    millilitre(s)
Pharmaceutical form:
  • Spot-on solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP53AX15
Authorisation status:
  • Surrendered
Authorised in:
  • Spain
Package description:
  • (ID6) 450 millilitre(s): Box (Cardboard) with 30 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 30 Pipette (PolyPropylene) each with 0.5 millilitre(s)
  • (ID5) 200 millilitre(s): Box (Cardboard) with 20 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 20 Pipette (PolyPropylene) each with 0.5 millilitre(s)
  • (ID4) 50 millilitre(s): Box (Cardboard) with 10 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 10 Pipette (PolyPropylene) each with 0.5 millilitre(s)
  • (ID3) 18 millilitre(s): Box (Cardboard) with 6 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 6 Pipette (PolyPropylene) each with 0.5 millilitre(s)
  • (ID2) 4.5 millilitre(s): Box (Cardboard) with 3 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 3 Pipette (PolyPropylene) each with 0.5 millilitre(s)
  • (ID1) 0.5 millilitre(s): Box (Cardboard) with Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) with 1 Pipette (PolyPropylene) with 0.5 millilitre(s)

Additional information

Entitlement type:
  • Marketing Authorisation
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:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 2404 ESP
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0189/001