Veterinary Medicines

Euthasol vet. 400 mg/ml, solution for injection

Authorised
  • Pentobarbital sodium
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Product identification

Medicine name:
Euthasol vet. 400 mg/ml, solution for injection
EUTHASOL, 400MG/ML SOLUZIONE INIETTABILE
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 sodium
    400.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intracardiac use
    • Cattle
    • Dog
    • Goat
    • Sheep
    • Horse (non food-producing)
    • Cat
    • Mink
    • Chinchilla
    • Gerbil
    • Guinea pig
    • Hamster
    • Mouse
    • Rat
    • Rabbit (non food-producing)
  • Intravenous use
    • Cattle
    • Dog
    • Goat
    • Sheep
    • Horse (non food-producing)
    • Cat
    • Mink
    • Chinchilla
    • Gerbil
    • Guinea pig
    • Hamster
    • Mouse
    • Rat
    • Rabbit (non food-producing)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN51AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:
  • 100 ml colourless type II glass vial with a light grey bromobutyl rubber stopper and an aluminium cap.
  • 250 ml colourless type II glass vial with a dark grey bromobutyl rubber stopper and an aluminium cap.

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:
  • Ministry Of Health
Authorisation number:
  • 104322
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)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 14/05/2022
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Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 3/06/2022
Download
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