Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Oprávnený
- Pentobarbital sodium
Identifikácia lieku
Názov lieku:
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Účinná látka:
- Dostupné len v English
Cieľové druhy:
Cesta podania:
-
Intrakardiálne použitie
-
Intravenózne použitie
-
Intraperitoneálne použitie
Podrobnosti o lieku
Účinná látka a sila:
-
Dostupné len v English400.00/milligram(s)1.00millilitre(s)
Lieková forma:
-
Injekčný roztok
Ochranná lehota podľa spôsobu podania:
-
Intrakardiálne použitie
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Cattle
-
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.
-
-
Horse
-
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.
-
-
Pig
-
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.
-
-
-
Intravenózne použitie
-
Cattle
-
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.
-
-
Horse
-
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.
-
-
Pig
-
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.
-
-
-
Intraperitoneálne použitie
-
Cattle
-
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.
-
-
Horse
-
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.
-
-
Pig
-
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.
-
-
Anatomicko-terapeuticko-chemický veterinárny kód (ATCvet):
- QN51AA01
Stav registrácie:
-
Valid
Registrovaný v/vo:
-
Poľsko
Opis balenia:
- Dostupné len v Poľsky
Ďalšie informácie
Anglicky:
Držiteľ rozhodnutia o registrácii:
- Biowet Pulawy Sp. z o.o.
Dátum registrácie lieku:
Miesta výroby na uvoľnenie šarže:
- Biowet Pulawy Sp. z o.o.
Zodpovedný orgán:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Číslo registrácie:
- 3218
Dátum zmeny stavu registrácie:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenty
Súhrn charakteristických vlastností lieku
Tento dokument v tomto jazyku (slovenčina) neexistuje. Nájdete ho v inom jazyku nižšie.
Poľsky (PDF)
Publikované na: 7/06/2023
Písomná informácia pre používateľa
Tento dokument v tomto jazyku (slovenčina) neexistuje. Nájdete ho v inom jazyku nižšie.
Poľsky (PDF)
Publikované na: 7/06/2023
Označenie obalu
Tento dokument v tomto jazyku (slovenčina) neexistuje. Nájdete ho v inom jazyku nižšie.
Poľsky (PDF)
Publikované na: 7/06/2023