Veterinary Medicines

Eliminall 50 mg spot-on solution for cats

Authorised
  • Fipronil
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Product identification

Medicine name:
Eliminall 50 mg spot-on solution for cats
Eliminall 50 mg Lösung zum Auftropfen für Katzen
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
Withdrawal period by route of administration:
  • Cutaneous use
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP53AX15
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
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
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:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 401445.00.00
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0189/001
Concerned member states:
  • Finland
  • Greece
  • Portugal
  • Spain

Documents

Summary of Product Characteristics

English (RTF)
Published on: 18/12/2024
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German (PDF)
Published on: 18/12/2024
Download

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 18/12/2024
Download

2401445-paren-20210316.pdf

English (PDF)
Published on: 18/12/2024
Download
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