T-61 SOLUCION INYECTABLE PARA INDUCCION DE LA EUTANASIA EN ANIMALES
T-61 SOLUCION INYECTABLE PARA INDUCCION DE LA EUTANASIA EN ANIMALES
Authorised
- Mebezonium iodide
- Embutramide
- Tetracaine hydrochloride
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
-
Ruminant
-
Ornamental bird
-
Fur animals
-
Laboratory animals
Route of administration:
-
Intravenous use
-
Intracardiac use
-
Intrapulmonary use
Product details
Active substance and strength:
-
Mebezonium iodide50.00/milligram(s)/millilitre1.00millilitre(s)
-
Embutramide200.00/milligram(s)/millilitre1.00millilitre(s)
-
Tetracaine hydrochloride5.00/milligram(s)/millilitre1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Horse
-
Meat and offalno withdrawal periodCarne: Se tomarán las medidas adecuadas para garantizar que los cuerpos de los animales muertos tratados con este medicamento veterinario y los subproductos de estos animales no entren en la cadena alimentaria y no se utilicen para el consumo humano o ani
-
-
Ruminant
-
Meat and offalno withdrawal periodCarne: Se tomarán las medidas adecuadas para garantizar que los cuerpos de los animales muertos tratados con este medicamento veterinario y los subproductos de estos animales no entren en la cadena alimentaria y no se utilicen para el consumo humano o ani
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN51AX50
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Available in:
-
Spain
Package description:
- Available only in Spanish
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:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 873 ESP
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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: 24/07/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 24/07/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 24/07/2024
