Dormostart 1 mg/ml solution for injection for dogs and cats
Dormostart 1 mg/ml solution for injection for dogs and cats
Authorised
- Medetomidine hydrochloride
Product identification
Medicine name:
Dormostart 1 mg/ml solution for injection for dogs and cats
Dormostart 1 mg/ml solution injectable pour chiens et chats
Dormostart 1 mg/ml oplossing voor injectie voor honden en katten
Dormostart 1 mg/ml Injektionslösung für Hunde und Katzen
Active substance:
- Medetomidine hydrochloride
Target species:
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Medetomidine hydrochloride1.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN05CM91
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 20 ml 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 5 ml (in a 10 ml sized vial) 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-V662141
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0401/001
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:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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in another language below.
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Dormostart, REG NL 130486 - Public Assessment Report - MEBa updated 20260126.pdf
English (PDF)
Download Published on: 26/01/2026