Veterinary Medicines

Euthasol 500 mg/ml solution for injection

Authorised
  • Pentobarbital sodium
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Product identification

Medicine name:
Euthasol 500 mg/ml solution for injection
Repose Vet. 500 mg/ml injektionsvæske, opløsning
Active substance:
  • Pentobarbital sodium
Target species:
  • Cattle
  • Dog
  • Goat (adult female)
  • Sheep
  • Horse
  • Cat
  • Rabbit
  • Mink
  • Rodents
  • Pig
Route of administration:
  • Intracardiac use
  • Intraperitoneal use
  • Intravenous use

Product details

Active substance and strength:
  • Pentobarbital sodium
    500.00
    milligram(s)
    /
    1.00
    millilitre(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:
  • Denmark
Package description:
  • 12 Clear Type I glass vials containing 100 ml, closed with a bromobutyl rubber stopper and aluminium cap in a carton box.
  • 12 Polypropylene vials containing 250 ml, closed with a bromobutyl rubber stopper and aluminium cap in a carton box.
  • 12 Clear Type I glass vials containing 250 ml, closed with a bromobutyl rubber stopper and aluminium cap in a carton box.
  • 1 Polypropylene vial containing 100 ml, closed with a bromobutyl rubber stopper and aluminium cap in a carton box.
  • 1 Clear Type I glass vial containing 250 ml, closed with a bromobutyl rubber stopper and aluminium cap in a carton box.
  • 1 Clear Type I glass vial containing 100 ml, closed with a bromobutyl rubber stopper and aluminium cap in a carton box.
  • 12 Polypropylene vials containing 100 ml, closed with a bromobutyl rubber stopper and aluminium cap in a carton box.
  • 1 Polypropylene vial containing 250 ml, closed with a bromobutyl rubber stopper and aluminium cap in a carton box.

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. Beheer B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Produlab Pharma B.V.
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 57731
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0320/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Malta
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Danish (, INJEKTIONSVÆSKE, OPLØSNING 500 MG-ML)
Published on: 7/04/2025
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Combined File of all Documents

English (PDF)
Published on: 20/02/2025
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