Veterinary Medicine Information website

Eliminall 134 mg spot-on solution for dogs

Not authorised
  • Fipronil
Download as PDF

Product identification

Medicine name:
Eliminall 134 mg spot-on solution for dogs
Active substance:
  • Fipronil
Target species:
  • Dog
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Fipronil
    134.00
    milligram(s)
    /
    1.34
    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:
  • Surrendered
Authorised in:
  • Spain
Package description:
  • (ID6) 1206 millilitre(s): Box (Cardboard) with 30 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 30 Pipette (PolyPropylene) each with 1.34 millilitre(s)
  • (ID5) 536 millilitre(s): Box (Cardboard) with 20 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 20 Pipette (PolyPropylene) each with 1.34 millilitre(s)
  • (ID4) 134 millilitre(s): Box (Cardboard) with 10 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 10 Pipette (PolyPropylene) each with 1.34 millilitre(s)
  • (ID3) 48.24 millilitre(s): Box (Cardboard) with 6 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 6 Pipette (PolyPropylene) each with 1.34 millilitre(s)
  • (ID2) 12.06 millilitre(s): Box (Cardboard) with 3 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 3 Pipette (PolyPropylene) each with 1.34 millilitre(s)
  • (ID1) 1.34 millilitre(s): Box (Cardboard) with Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) 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:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 2406 ESP
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0189/003

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 14/03/2026
Download

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 14/03/2026
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 14/03/2026
Download