Veterinary Medicine Information website

Ataxxa 2000 mg/400 mg spot-on solution for dogs over 25 kg

Authorised
  • Permethrin
  • Imidacloprid
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Product identification

Medicine name:
Ataxxa 2000 mg/400 mg spot-on solution for dogs over 25 kg
Active substance:
  • Permethrin
  • Imidacloprid
Target species:
  • Dog
Route of administration:
  • Spot-on use

Product details

Active substance and strength:
  • Permethrin
    2000.00
    milligram(s)
    /
    1.00
    Pipette
  • Imidacloprid
    400.00
    milligram(s)
    /
    1.00
    Pipette
Pharmaceutical form:
  • Spot-on solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP53AC54
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Available in:
  • Slovakia
Package description:
  • White polypropylene pipette closed with a polyethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 1 pipettes.
  • White polypropylene pipette closed with a polyethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 3 pipettes.
  • White polypropylene pipette closed with a polyethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 4 pipettes.
  • White polypropylene pipette closed with a polyethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 6 pipettes.
  • White polypropylene pipette closed with a polyethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 10 pipettes.
  • White polypropylene pipette closed with a polyoxymethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 1 pipettes.
  • White polypropylene pipette closed with a polyoxymethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 3 pipettes.
  • White polypropylene pipette closed with a polyoxymethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 4 pipettes.
  • White polypropylene pipette closed with a polyoxymethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 6 pipettes.
  • White polypropylene pipette closed with a polyoxymethylene cap. Each pipette is packed in apolyethylene terephthalate/aluminium/low density polyethylene triplex bag.6 ml pipette containing 4 ml of solutionBox containing 10 pipettes.

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
  • TAD Pharma GmbH
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/065/DC/15-S
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0439/004
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Czechia
  • Estonia
  • France
  • Germany
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 4/10/2023
Updated on: 6/10/2023
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Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
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English (PDF)
Published on: 30/06/2024
Updated on: 13/03/2026
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