Veterinary Medicines Information website

NexGard Combo 10.8 mg + 3.6 mg + 74.7 mg - Spot-on solution

Authorised
  • Esafoxolaner
  • Eprinomectin
  • Praziquantel
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Product identification

Medicine name:
NexGard Combo 10.8 mg + 3.6 mg + 74.7 mg - Spot-on solution
Active substance:
  • Esafoxolaner
  • Eprinomectin
  • Praziquantel
Target species:
  • Cat
Route of administration:
  • Spot-on use

Product details

Active substance and strength:
  • Esafoxolaner
    Presentation_strength:10.8 mg Reference:Hse Index:0
  • Eprinomectin
    Presentation_strength:3.6 mg Reference:Hse Index:1
  • Praziquantel
    Presentation_strength:74.7 mg Reference:Ph.Eur. Index:2
Pharmaceutical form:
  • Spot-on solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA54
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Available in:
  • Austria
  • Belgium
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Latvia
  • Lithuania
  • Luxembourg
  • Norway
  • Poland
  • Slovakia
  • Spain
  • Sweden
Package description:
  • Packaging:Spot-on applicator (COC), Package_size:15 applicators, Content:0.9 ml
  • Packaging:Spot-on applicator (COC), Package_size:6 applicators, Content:0.9 ml
  • Packaging:Spot-on applicator (COC), Package_size:4 applicators, Content:0.9 ml
  • Packaging:Spot-on applicator (COC), Package_size:1 applicator, Content:0.9 ml
  • Packaging:Spot-on applicator (COC), Package_size:3 applicators, Content:0.9 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Fixed combination application (Article 13b of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • European Commission
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

English (PDF)
Published on: 13/03/2026
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Czech (PDF)
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Danish (PDF)
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German (PDF)
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Greek (PDF)
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Bulgarian (PDF)
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Spanish (PDF)
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Estonian (PDF)
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Finnish (PDF)
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French (PDF)
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Croatian (PDF)
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Hungarian (PDF)
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Icelandic (PDF)
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Italian (PDF)
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Lithuanian (PDF)
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Latvian (PDF)
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Maltese (PDF)
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Dutch (PDF)
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Polish (PDF)
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Romanian (PDF)
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Slovak (PDF)
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Slovenian (PDF)
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Swedish (PDF)
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Norwegian (PDF)
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Portuguese (PDF)
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ema-puar-v5094-nexgard-combo-vra0007g-en.pdf

English (PDF)
Published on: 14/03/2026
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ema-puar-nexgard-combo-v-5094-var-ii-0002-g-en.pdf

English (PDF)
Published on: 14/03/2026
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ema-puar-nexgard-combo-v-5094-par-en.pdf

English (PDF)
Published on: 14/03/2026
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ema-puar-v5094-nexgardcombo-vra0012g-en.pdf

English (PDF)
Published on: 13/03/2026
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