T 61 Oplossing voor injectie
T 61 Oplossing voor injectie
Autorizado
- Mebezonium iodide
- Embutramide
- Tetracaine hydrochloride
Identificação do produto
Nome do medicamento veterinário:
T 61 Oplossing voor injectie
T 61 Solution injectable
T 61 Injektionslösung
Espécies-alvo:
Via de administração:
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Via intrapulmonar
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Via intracardíaca
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Via intravenosa
Detalhes do medicamento veterinário
Forma farmacêutica:
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Solução injetável
Intervalo de segurança por via de administração:
-
Via intrapulmonar
-
Dog
-
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
-
-
Cat
-
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
-
-
Mink
-
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
-
-
Ornamental bird
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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
-
-
Laboratory animals
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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
-
-
Pigeon
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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
-
-
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Via intracardíaca
-
Dog
-
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
-
-
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Via intravenosa
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Cattle
-
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
-
-
Horse
-
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
-
-
Dog
-
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 Anatomical Therapeutic Chemical Code (ATCvet):
- QN51AX50
Classificação quanto à dispensa:
-
Medicamento veterinário sujeito a prescrição veterinária
Estado da autorização:
-
Autorizado
Autorisado em:
-
Bélgica
Descrição da embalagem:
- Disponível apenas em inglês
Informações adicionais
Titular da autorização de introdução no mercado:
- Intervet International B.V.
Data de autorização de introdução no mercado:
Locais de fabrico para a libertação de lotes:
- Intervet International GmbH
Autoridade responsável:
- Federal Agency For Medicines And Health Products
Número da autorização:
- BE-V179304
Data da alteração do estado de autorização:
Para consultar as notificações de suspeitas de eventos adversos: www.adrreports.eu/vet
Documentos
Resumo das características do medicamento
Este documento não existe neste idioma (português). Você pode encontrá -lo em outro idioma abaixo.
francês (PDF)
Publicado em: 18/08/2025
neerlandês (PDF)
Publicado em: 18/08/2025
Folheto informativo
Este documento não existe neste idioma (português). Você pode encontrá -lo em outro idioma abaixo.
alemão (PDF)
Publicado em: 18/08/2025
francês (PDF)
Publicado em: 18/08/2025
neerlandês (PDF)
Publicado em: 18/08/2025
Rotulagem
Este documento não existe neste idioma (português). Você pode encontrá -lo em outro idioma abaixo.
alemão (PDF)
Publicado em: 18/08/2025
francês (PDF)
Publicado em: 18/08/2025
neerlandês (PDF)
Publicado em: 18/08/2025
