Euthasol vet. 400 mg/ml, solution for injection
Euthasol vet. 400 mg/ml, solution for injection
Authorised
- Pentobarbital sodium
Product identification
Medicine name:
Euthasol vet. 400 mg/ml, solution for injection
EUTHASOL 400 mg/ml SOLUCION INYECTABLE
Active substance:
- Pentobarbital sodium
Target species:
-
Cattle
-
Dog
-
Goat
-
Sheep
-
Horse (non food-producing)
-
Cat
-
Mink
-
Chinchilla
-
Gerbil
-
Guinea pig
-
Hamster
-
Mouse
-
Rat
-
Rabbit (non food-producing)
Route of administration:
-
Intracardiac use
-
Intravenous use
Product details
Active substance and strength:
-
Pentobarbital sodium400.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN51AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Package description:
- 100 ml colourless type I glass vial with a light grey bromobutyl rubber stopper and an aluminium cap.
- 250 ml colourless type I glass vial with a dark grey bromobutyl rubber stopper and an aluminium cap.
- 100 ml colourless type II glass vial with a light grey bromobutyl rubber stopper and an aluminium cap. [HISTORICAL]
- 250 ml colourless type II glass vial with a dark grey bromobutyl rubber stopper and an aluminium cap. [HISTORICAL]
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Le Vet. B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Produlab Pharma B.V.
Responsible authority:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 2455 ESP
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0618/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
Estonia
-
Finland
-
France
-
Greece
-
Iceland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Norway
-
Poland
-
Portugal
-
Romania
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 28/01/2022
Spanish (PDF)
Published on: 6/08/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 6/08/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 6/08/2025
Combined File of all Documents
English (PDF)
Download Published on: 6/07/2025