T 61 Oplossing voor injectie
T 61 Oplossing voor injectie
Autorisert
- Mebezonium iodide
- Embutramide
- Tetracaine hydrochloride
Produkt identifikasjon
Legemidlets navn:
T 61 Oplossing voor injectie
T 61 Solution injectable
T 61 Injektionslösung
Administrasjonsvei:
-
Intrapulmonal bruk
-
Intrakardial bruk
-
Intravenøs bruk
Produktdetaljer
Legemiddelform:
-
Injeksjonsvæske, oppløsning
Tilbakeholdelsestid etter administrasjonsvei:
-
Intrapulmonal bruk
-
hund
-
Slaktno 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
-
-
katt
-
Slaktno 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
-
Slaktno 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
-
-
prydfugl
-
Slaktno 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
-
Slaktno 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
-
-
due
-
Slaktno 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
-
-
-
Intrakardial bruk
-
hund
-
Slaktno 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
-
-
-
Intravenøs bruk
-
storfe
-
Slaktno 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
-
-
hest
-
Slaktno 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
-
-
hund
-
Slaktno 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
-
-
Anatomisk terapeutisk kjemisk klassifisering for veterinærpreparater (ATCvet):
- QN51AX50
Juridisk status for forsyning
:
-
Veterinært legemiddel gjenstand for veterinær forskrivning
Status for markedsføringstillatelse:
-
Gyldig
Autorisert i:
-
BE
Pakningsbeskrivelse:
- Bare tilgjengelig i English
Tilleggsinformasjon
Rettighetstype:
-
Marketing Authorisation
Innehaver av markedsføringstillatelse:
- Intervet International B.V.
Markedsføringsgodkjenningsdato:
Tilvirker for batchfrigivelse:
- Intervet International GmbH
Ansvarlig myndighet:
- Federal Agency For Medicines And Health Products
Godkjenningsnummer:
- BE-V179304
Status for endring av markedsføringstillatelse:
Rapporter om mistenkte bivirkninger: www.adrreports.eu/vet
Dokumenter
Preparatomtale
Dette dokumentet eksisterer ikke på dette språket (Norsk). Du kan finne det på et annet språk nedenfor.
Dutch (PDF)
Publisert på: 14/10/2024
French (PDF)
Publisert på: 14/10/2024
Pakningsvedlegg
Dette dokumentet eksisterer ikke på dette språket (Norsk). Du kan finne det på et annet språk nedenfor.
Dutch (PDF)
Publisert på: 14/10/2024
French (PDF)
Publisert på: 14/10/2024
German (PDF)
Publisert på: 14/10/2024
Merking
Dette dokumentet eksisterer ikke på dette språket (Norsk). Du kan finne det på et annet språk nedenfor.
French (PDF)
Publisert på: 14/10/2024
German (PDF)
Publisert på: 14/10/2024
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