Veterinary Medicines

Alizin 30 mg/ml Solution for Injection

Authorised
  • Aglepristone
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Product identification

Medicine name:
Alizin 30 mg/ml Solution for Injection
Alizin 30 mg/ml Oplossing voor injectie
Alizin 30 mg/ml Solution injectable
Alizin 30 mg/ml Injektionslösung
Active substance:
  • Aglepristone
Target species:
  • Dog
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Aglepristone
    30.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG03XB90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • Vial (glass, type II) of 5 ml for injectable preparation, with bromobutyl stopper and aluminum cap.Presentation:- box of 1 vial of 5ml
  • Vial (glass, type II) of 10 ml for injectable preparation, with bromobutyl stopper and aluminum cap.Presentation:- box of 1 vial of 10ml.
  • Vial (glass, type II) of 30 ml for injectable preparation, with bromobutyl stopper and aluminum cap.Presentation:- box of 1 vial of 30ml.
  • Vials (glass, type II) of 10 ml for injectable preparations, with bromobutyl stoppers and aluminum caps.Presentation:- box of 10 vials of 10ml.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
  • Virbac
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V263986
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0500/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 16/11/2025
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Dutch (PDF)
Published on: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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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: 18/08/2025
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French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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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: 18/08/2025
Download
French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Combined File of all Documents

English (PDF)
Published on: 16/11/2025
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