T 61 Oplossing voor injectie
T 61 Oplossing voor injectie
Authorised
- Tetracaine hydrochloride
- Embutramide
- Mebezonium iodide
Produktidentifikasjon
Legemidlets navn:
T 61 Oplossing voor injectie
T 61 Solution injectable
T 61 Injektionslösung
Administrering:
-
Intrapulmonal bruk
-
Intrakardial bruk
-
Intravenøs bruk
Produktdetaljer
Legemiddelform:
-
Injeksjonsvæske, oppløsning
Withdrawal period by route of administration:
-
Intrapulmonary use
- 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
-
-
Intracardiac use
- 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
-
-
Intravenous use
- 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
Utleveringsbestemmelser
:
-
Veterinært legemiddel gjenstand for veterinær forskrivning
Status for markedsføringstillatelse:
-
Gyldig
Authorised in:
-
BE
Pakningsvedlegg:
- Tilgjengelig bare i English
Mer informasjon
Entitlement type:
-
Markedsføringstillatelse
Innehaver av markedsføringstillatelse:
- Intervet International B.V.
Marketing authorisation date:
Tilvirker ansvarlig for batchfrigivelse:
- Intervet International GmbH
Ansvarlig myndighet:
- FAMHP
Godkjenningsnummer:
- BE-V179304
Dato for endring av status for markedsføringstillatelse:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenter
Preparatomtale
Dette dokumentet eksisterer ikke på dette språket (Norwegian). Du kan finne det på et annet språk nedenfor.
Dutch (PDF)
Publisert på: 22/03/2022
French (PDF)
Publisert på: 22/03/2022
Pakningsvedlegg
Dette dokumentet eksisterer ikke på dette språket (Norwegian). Du kan finne det på et annet språk nedenfor.
Dutch (PDF)
Publisert på: 22/03/2022
French (PDF)
Publisert på: 22/03/2022
German (PDF)
Publisert på: 22/03/2022
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