Veterinary Medicines

Euthoxin 500 mg/ml Solution for Injection

Authorised
  • Pentobarbital sodium
  • Pentobarbital sodium
  • Pentobarbital sodium
  • Pentobarbital sodium
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Product identification

Medicine name:
Euthoxin 500 mg/ml solution for injection
Euthoxin 500 mg/ml Solution for Injection
Active substance:
  • Pentobarbital sodium
  • Pentobarbital sodium
  • Pentobarbital sodium
  • Pentobarbital sodium
Target species:
  • Dog
  • Cat
  • Mink
  • Ferret
  • Hare
  • Rabbit
  • Guinea pig
  • Hamster
  • Rat
  • Chicken
  • Homing pigeon
  • Ornamental bird
  • Snake
  • Turtle
  • Lizard
  • Frog
  • Horse
  • Cattle
  • Pig
  • Dog
  • Cat
  • Mink
  • Ferret
  • Hare
  • Rabbit
  • Guinea pig
  • Hamster
  • Rat
  • Chicken
  • Homing pigeon
  • Ornamental bird
  • Snake
  • Turtle
  • Lizard
  • Frog
  • Horse
  • Cattle
  • Pig
  • Dog
  • Cat
  • Mink
  • Ferret
  • Hare
  • Rabbit
  • Guinea pig
  • Hamster
  • Rat
  • Chicken
  • Homing pigeon
  • Ornamental bird
  • Snake
  • Turtle
  • Lizard
  • Frog
  • Horse
  • Cattle
  • Pig
  • Dog
  • Cat
  • Mink
  • Ferret
  • Hare
  • Rabbit
  • Guinea pig
  • Hamster
  • Rat
  • Chicken
  • Homing pigeon
  • Ornamental bird
  • Snake
  • Turtle
  • Lizard
  • Frog
  • Horse
  • Cattle
  • Pig
Route of administration:
  • Intravenous use
  • Intracardiac use
  • Intraperitoneal use
  • Intrapulmonary use

Product details

Active substance and strength:
  • Pentobarbital sodium
    500.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Pentobarbital sodium
    500.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Pentobarbital sodium
    500.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • 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:
  • United Kingdom (Northern Ireland)
Package description:
  • 100 ml Type I amber multi-dose glass vials closed with a bromobutyl rubber stopper and sealed with an aluminium overseal. The product is presented in a carton.

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:
  • Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 08749/4055
Date of authorisation status change:
Reference member state:
  • Portugal
Procedure number:
  • PT/V/0142/001
Concerned member states:
  • Austria
  • Belgium
  • Croatia
  • France
  • Greece
  • Hungary
  • Ireland
  • Netherlands
  • Norway
  • Romania
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 19/05/2025
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