Veterinary Medicines

T-61 SOLUCION INYECTABLE PARA INDUCCION DE LA EUTANASIA EN ANIMALES

Authorised
  • Mebezonium iodide
  • Embutramide
  • Tetracaine hydrochloride
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Product identification

Medicine name:
T-61 SOLUCION INYECTABLE PARA INDUCCION DE LA EUTANASIA EN ANIMALES
Active substance:
  • Mebezonium iodide
  • Embutramide
  • Tetracaine hydrochloride
Target species:
  • Horse
  • Dog
  • Cat
  • Ornamental bird
  • Ruminant
  • Fur animals
  • Laboratory animals
Route of administration:
  • Intracardiac use
  • Intrapleural use
  • Intravenous use

Product details

Active substance and strength:
  • Mebezonium iodide
    50.00
    milligram(s)/millilitre
    /
    1.00
    millilitre(s)
  • Embutramide
    200.00
    milligram(s)/millilitre
    /
    1.00
    millilitre(s)
  • Tetracaine hydrochloride
    5.00
    milligram(s)/millilitre
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intracardiac use
    • Horse
      • Meat and offal
        no withdrawal period
    • Dog
    • Cat
    • Ornamental bird
    • Ruminant
      • Meat and offal
        no withdrawal period
    • Fur animals
    • Laboratory animals
  • Intrapleural use
    • Horse
      • Meat and offal
        no withdrawal period
    • Dog
    • Cat
    • Ornamental bird
    • Ruminant
      • Meat and offal
        no withdrawal period
    • Fur animals
    • Laboratory animals
  • Intravenous use
    • Horse
      • Meat and offal
        no withdrawal period
    • Dog
    • Cat
    • Ornamental bird
    • Ruminant
      • Meat and offal
        no withdrawal period
    • Fur animals
    • Laboratory animals
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN51AX50
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Spain
Package description:

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:
  • Merck Sharp & Dohme Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International GmbH
Responsible authority:
  • The Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 873 ESP
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 1/02/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 1/02/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 1/02/2024
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