Sedator, 1.0 mg/ml, solution for injection for cats and dogs
Sedator, 1.0 mg/ml, solution for injection for cats and dogs
Authorised
- Medetomidine hydrochloride
Product identification
Medicine name:
Sedator, 1.0 mg/ml, solution for injection for cats and dogs
SEDATOR 1,0 mg/ml raztopina za injiciranje za mačke in pse
Active substance:
- Medetomidine hydrochloride
Target species:
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Medetomidine hydrochloride1.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Dog
-
Cat
-
-
Intravenous use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN05CM91
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Package description:
- (ID3) 20 millilitre(s): unspecified outer container with 1 Vial with 20 millilitre(s)
- (ID2) 10 millilitre(s): unspecified outer container with 1 Vial with 10 millilitre(s)
- (ID1) 5 millilitre(s): unspecified outer container with 1 Vial with 5 millilitre(s)
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:
- Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- MR/V/0312/001
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0119/001
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Finland
-
France
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 2/03/2022
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 2/03/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 2/03/2022
Combined File of all Documents
English (PDF)
Download Published on: 23/10/2024
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