Veterinary Medicine Information website

Dexdormostart 0.5 mg/ml solution for injection for dogs and cats

Authorised
  • Dexmedetomidine hydrochloride
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Product identification

Medicine name:
Dexdormostart 0.5 mg/ml solution for injection for dogs and cats
Active substance:
  • Dexmedetomidine hydrochloride
Target species:
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Dexmedetomidine hydrochloride
    0.50
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN05CM18
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Cardboard box with one clear Type I glass vial of 5 ml (in a 10 ml sized vial) with grey fluorinated coated bromobutyl rubber stopper and aluminium cap.
  • Cardboard box with one clear Type I glass vial of 10 ml with grey fluorinated coated bromobutyl rubber stopper and aluminium cap.
  • Cardboard box with one clear Type I glass vial of 20 ml with grey fluorinated coated bromobutyl rubber stopper and aluminium cap.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Alfasan Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Alfasan Nederland B.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V662140
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0400/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Generic of:

Documents

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
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German (PDF)
Published on: 18/08/2025
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French (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: 23/03/2026
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German (PDF)
Published on: 23/03/2026
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French (PDF)
Published on: 23/03/2026
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Summary of Product Characteristics

English (PDF)
Published on: 25/03/2026
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French (PDF)
Published on: 23/03/2026
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Dutch (PDF)
Published on: 23/03/2026
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German (PDF)
Published on: 23/03/2026
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Combined File of all Documents

English (PDF)
Published on: 14/03/2026
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PuAR Dexdormostart NL-V-0400-001-DC.pdf

English (PDF)
Published on: 24/11/2023
Updated on: 14/03/2026
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