Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Autorizat
- Pentobarbital sodium
Identificarea produsului
Denumirea medicamentului:
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Substanța activă:
- Disponibile numai în Engleză
Specia țintă:
-
Bovine
-
Cal
-
Porc
-
Câine
-
Pisică
Calea de administrare:
-
Administrare intracardiacă
-
Administrare intravenoasă
-
Administrare intraperitoneală
Detalii produs
Substanța activă și concentraţie:
-
Disponibile numai în Engleză400.00/miligram(e)1.00mililitru(i)
Forma farmaceutică:
-
Soluţie injectabilă
Perioada de așteptare în funcție de calea administrare:
-
Administrare intracardiacă
-
Bovine
-
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.
-
-
Cal
-
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.
-
-
Porc
-
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.
-
-
-
Administrare intravenoasă
-
Bovine
-
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.
-
-
Cal
-
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.
-
-
Porc
-
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.
-
-
-
Administrare intraperitoneală
-
Bovine
-
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.
-
-
Cal
-
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.
-
-
Porc
-
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.
-
-
Codul anatomic terapeutic chimic veterinar (ATCvet):
- QN51AA01
Statusul legal privind eliberarea:
-
Produs medicinal veterinar care se eliberează cu prescripție veterinară
Status autorizaţie:
-
Valid
Descrierea ambalajului:
- Disponibile numai în Poloneză
Informații suplimentare
Deținătorul autorizației de comercializare:
- Biowet Pulawy Sp. z o.o.
Data autorizației de comercializare:
Producătorul responsabil pentru eliberarea seriei:
- Biowet Pulawy Sp. z o.o.
Autoritatea responsabilă:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Numărul autorizației:
- 3218
Data modificării statusului autorizației:
Pentru a consulta reacțiile adverse la produsele medicinale veterinare, vă rugăm să accesați www.adrreports.eu/vet
Documente
Rezumatul caracteristicilor produsului
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Poloneză (PDF)
Publicat la: 7/06/2023
Prospectul
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Poloneză (PDF)
Publicat la: 7/06/2023
Etichetarea
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Poloneză (PDF)
Publicat la: 7/06/2023