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Veterinary Medicines

T 61 Oplossing voor injectie

Authorised
  • Mebezonium iodide
  • Embutramide
  • Tetracaine hydrochloride

Product identification

Medicine name:
T 61 Oplossing voor injectie
T 61 Solution injectable
T 61 Injektionslösung
Active substance:
  • Mebezonium iodide
  • Embutramide
  • Tetracaine hydrochloride
Target species:
  • Dog
  • Cat
  • Mink
  • Ornamental bird
  • Laboratory animals
  • Pigeon
  • Cattle
  • Horse
Route of administration:
  • Intrapulmonary use
  • Intracardiac use
  • Intravenous use

Product details

Active substance and strength:
  • Mebezonium iodide
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Embutramide
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Tetracaine hydrochloride
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intrapulmonary use
    • Dog
      • Meat and offal
        no withdrawal period
    • Cat
      • Meat and offal
        no withdrawal period
    • Mink
      • Meat and offal
        no withdrawal period
    • Ornamental bird
      • Meat and offal
        no withdrawal period
    • Laboratory animals
      • Meat and offal
        no withdrawal period
    • Pigeon
      • Meat and offal
        no withdrawal period
  • Intracardiac use
    • Dog
      • Meat and offal
        no withdrawal period
  • Intravenous use
    • Cattle
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
    • Dog
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN51AX50
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • T 61 50 ml Vial Solution for injection

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International GmbH
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V179304
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.
Dutch (PDF)
Published on: 18/08/2025
French (PDF)
Published on: 18/08/2025

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
French (PDF)
Published on: 18/08/2025
German (PDF)
Published on: 18/08/2025

Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/08/2025
French (PDF)
Published on: 18/08/2025
German (PDF)
Published on: 18/08/2025