T 61 Oplossing voor injectie
T 61 Oplossing voor injectie
Autorizado
- Mebezonium iodide
- Embutramide
- Tetracaine hydrochloride
Identificación del medicamento
Nombre del medicamento:
T 61 Oplossing voor injectie
T 61 Solution injectable
T 61 Injektionslösung
Especies de destino:
-
Perros
-
Gatos
-
Visones
-
Aves ornamentales
-
Animales de laboratorio
-
Palomas
-
Bovino
-
Caballos
Vía de administración:
-
Uso intrapulmonar
-
Vía intracardiaca
-
Vía intravenosa
Datos del medicamento
Forma farmacéutica:
-
Solución inyectable
Tiempo de espera por vía de administración:
-
Uso intrapulmonar
-
Perros
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Gatos
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Visones
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Aves ornamentales
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Animales de laboratorio
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Palomas
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
-
Vía intracardiaca
-
Perros
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
-
Vía intravenosa
-
Bovino
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Caballos
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
Perros
-
Meat and offalno withdrawal periodEuthanised animals should not be used as food (animal or human). Adequate measures should be taken to ensure that carcasses of animals treated with this product and the by-products of these animals do not enter the food chain and are not used for human or animal consumption
-
-
código químico anatómico-terapéutico para medicamentos veterinarios (ATCvet):
- QN51AX50
Estado de la autorización:
-
Autorizado
Autorizado en:
-
Bélgica
Descripción del formato:
- Disponible únicamente en English
Información adicional
Titular de la autorización de comercialización:
- Intervet International B.V.
Fecha de autorización de comercialización:
Fabricante responsable de la liberación del lote:
- Intervet International GmbH
Autoridad responsable:
- Federal Agency For Medicines And Health Products
Número de autorización:
- BE-V179304
Fecha de modificación del estado de la autorización:
Para consultar notificaciones de presuntos efectos adversos diríjase a www.adrreports.eu/vet
Documentos
Ficha técnica o resumen de las características del producto
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Prospecto
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Etiquetado
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