Veterinary Medicines

Euthanimal 40%

Authorised
  • Pentobarbital sodium
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Product identification

Medicine name:
Euthanimal 40%
Euthanimal vet 400 mg/ml Injektionsvätska, lösning
Active substance:
  • Pentobarbital sodium
Target species:
  • Cattle
  • Dog
  • Goat (adult female)
  • Sheep
  • Horse
  • Cat
  • Pig
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 (adult female)
    • Sheep
    • Horse
    • Cat
    • Pig
  • Intravenous use
    • Cattle
    • Dog
    • Goat (adult female)
    • Sheep
    • Horse
    • Cat
    • Pig
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN51AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Sweden
Package description:
  • 1 vial of 100 ml, type II glass injection vial with a bromobutylrubber stopper and aluminium cap in carton box.
  • 6 vials of 250 ml, type II glass injection vial with a bromobutylrubber stopper and aluminium cap in polystyrene box.
  • 12 vials of 100 ml, type II glass injection vial with a bromobutylrubber stopper and aluminium cap in polystyrene box.
  • 1 vial of 250 ml, type II glass injection vial with a bromobutylrubber stopper and aluminium cap in carton box.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Alfasan Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Alfasan Nederland B.V.
Responsible authority:
  • Swedish Medical Products Agency
Authorisation number:
  • 49155
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0177/002
Concerned member states:
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Malta
  • Poland
  • Portugal
  • Romania
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 2/05/2022
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 2/05/2022
Download
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