Veterinary Medicines

Milprazon 4 mg/10 mg film-coated tablets for small cats and kittens weighing at least 0.5 kg

Authorised
  • Milbemycin oxime
  • Praziquantel
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Product identification

Medicine name:
Milprazon 4 mg/10 mg film-coated tablets for small cats and kittens weighing at least 0.5 kg
Milprazon 4 mg - 10 mg Filmomhulde tablet
Milprazon 4 mg - 10 mg Comprimé pelliculé
Milprazon 4 mg - 10 mg Filmtablette
Active substance:
  • Milbemycin oxime
  • Praziquantel
Target species:
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Milbemycin oxime
    4.00
    milligram(s)
    /
    1.00
    Tablet
  • Praziquantel
    10.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Film-coated tablet
Withdrawal period by route of administration:
  • Oral use
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AB51
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Blister packs consisting of cold formed OPA/Al/PVC foil and aluminium foil. Box with 1 blister of 2 tablets.
  • Blister packs consisting of cold formed OPA/Al/PVC foil and aluminium foil. Box with 1 blister of 4 tablets.
  • Blister packs consisting of cold formed OPA/Al/PVC foil and aluminium foil. Box with 12 blisters, each blister contains 4 tablets.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) 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
  • Krka-Farma d.o.o.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V474017
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0464/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 26/08/2024
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Dutch (PDF)
Published on: 14/03/2025
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French (PDF)
Published on: 14/03/2025
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German (PDF)
Published on: 14/03/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 14/03/2025
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French (PDF)
Published on: 14/03/2025
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German (PDF)
Published on: 14/03/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 14/03/2025
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French (PDF)
Published on: 14/03/2025
Download
German (PDF)
Published on: 14/03/2025
Download
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