Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Autorizado
- Pentobarbital sodium
Identificación del medicamento
Nombre del medicamento:
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Principio activo:
- Disponible únicamente en English
Especies de destino:
-
Bovino
-
Caballos
-
Porcino
-
Perros
-
Gatos
Vía de administración:
-
Vía intracardiaca
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Vía intravenosa
-
Vía intraperitoneal
Datos del medicamento
Principio activo y concentración:
-
Disponible únicamente en English400.00/Miligramo(s)1.00Mililitro(s)
Forma farmacéutica:
-
Solución inyectable
Tiempo de espera por vía de administración:
-
Vía intracardiaca
-
Bovino
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Caballos
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Porcino
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
-
Vía intravenosa
-
Bovino
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Caballos
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Porcino
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
-
Vía intraperitoneal
-
Bovino
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Caballos
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
Porcino
-
All relevant tissuesno withdrawal periodNot applicable. Appropriate measures must be taken to ensure that tissues of animals that have received this product, as well as animal by-products derived from these animals, do not enter the food chain and are not used for consumption by humans or other animals.
-
-
código químico anatómico-terapéutico para medicamentos veterinarios (ATCvet):
- QN51AA01
Estado de la autorización:
-
Autorizado
Autorizado en:
-
Polonia
Descripción del formato:
- Disponible únicamente en Polish
Información adicional
Titular de la autorización de comercialización:
- Biowet Pulawy Sp. z o.o.
Fecha de autorización de comercialización:
Fabricante responsable de la liberación del lote:
- Biowet Pulawy Sp. z o.o.
Autoridad responsable:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Número de autorización:
- 3218
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
Este documento no existe en este idioma (Español). Puede encontrarlo en otro idioma a continuación.
Polish (PDF)
Publicado el: 7/06/2023
Prospecto
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Polish (PDF)
Publicado el: 7/06/2023
Etiquetado
Este documento no existe en este idioma (Español). Puede encontrarlo en otro idioma a continuación.
Polish (PDF)
Publicado el: 7/06/2023