Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Godkänd
- Pentobarbital sodium
Produktbeteckning
Läkemedlets namn:
Morbital Plus 400 mg/1 ml roztwór do wstrzykiwań
Aktiv substans:
- Finns tillgänglig endast på engelska
Djurslag:
-
Nöt
-
Häst
-
Svin
-
Hund
-
Katt
Administreringsväg:
-
Intrakardiell användning
-
Intravenös användning
-
Intraperitoneal användning
Ytterligare information om produkten
Aktiv substans och styrka:
-
Finns tillgänglig endast på engelska400.00/milligram(s)1.00millilitre(s)
Läkemedelsform:
-
Injektionsvätska, lösning
Karenstid per administreringsväg:
-
Intrakardiell användning
-
Nöt
-
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.
-
-
Häst
-
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.
-
-
Svin
-
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.
-
-
-
Intravenös användning
-
Nöt
-
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.
-
-
Häst
-
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.
-
-
Svin
-
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.
-
-
-
Intraperitoneal användning
-
Nöt
-
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.
-
-
Häst
-
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.
-
-
Svin
-
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.
-
-
Anatomisk terapeutisk kemisk veterinärkod (ATCvet-kod):
- QN51AA01
Receptstatus:
-
Receptbelagt veterinärmedicinskt läkemedel
Godkännandestatus:
-
Godkänd
Godkänd i:
-
Polen
Förpackningsbeskrivning:
- Finns tillgänglig endast på polska
Ytterligare information
Typ av berättigande:
-
Marketing Authorisation
Legal grund för produktgodkännande:
Innehavare av godkännande för försäljning:
- Biowet Pulawy Sp. z o.o.
Godkännandedatum:
Tillverkningsplatser för frisläppande av tillverkningssatser:
- Biowet Pulawy Sp. z o.o.
Ansvarig myndighet:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Godkännandenummer:
- 3218
Datum för ändring av godkännandestatus:
Rapporter om misstänkta biverkningar: www.adrreports.eu/vet
Dokument
Produktresumé
Det här dokumentet finns inte på detta språk (svenska). Du kan hitta det på ett annat språk nedan.
polska (PDF)
Publicerad på: 7/06/2023
Bipacksedel
Det här dokumentet finns inte på detta språk (svenska). Du kan hitta det på ett annat språk nedan.
polska (PDF)
Publicerad på: 7/06/2023
Märkningstext
Det här dokumentet finns inte på detta språk (svenska). Du kan hitta det på ett annat språk nedan.
polska (PDF)
Publicerad på: 7/06/2023