T 61 Oplossing voor injectie
T 61 Oplossing voor injectie
Heimilað
- Mebezonium iodide
- Embutramide
- Tetracaine hydrochloride
Auðkenni lyfs
Heiti lyfs:
T 61 Oplossing voor injectie
T 61 Solution injectable
T 61 Injektionslösung
Leið stjórnsýslu:
-
Til notkunar í lungu
-
Til notkunar í hjarta
-
Til notkunar í bláæð
Upplýsingar um lyf
Lyfjaform:
-
Stungulyf, lausn
Afurðanýtingafrestur eftir íkomuleið:
-
Til notkunar í lungu
-
Hundur
-
Kjöt og innmaturno 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
-
-
Köttur
-
Kjöt og innmaturno 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
-
-
Minkur
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Kjöt og innmaturno 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
-
-
Skrautfugl
-
Kjöt og innmaturno 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
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Kjöt og innmaturno 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
-
-
Dúfa
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Kjöt og innmaturno 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
-
-
-
Til notkunar í hjarta
-
Hundur
-
Kjöt og innmaturno 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
-
-
-
Til notkunar í bláæð
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Nautgripir
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Kjöt og innmaturno 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
-
-
Hestur
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Kjöt og innmaturno 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
-
-
Hundur
-
Kjöt og innmaturno 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
-
-
ATC flokkun (dýralyf) (e. Anatomical therapeutic chemical veterinary - ATC-VET):
- QN51AX50
Lögformleg staða:
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Ávísunarskylt dýralyf
Staða leyfis:
-
Gilt
Heimilað í:
-
Belgía
Lýsing umbúða:
- Aðeins fáanlegt í enska
Aðrar upplýsingar
Réttindategund:
-
Marketing Authorisation
Markaðsleyfishafi:
- Intervet International B.V.
Dagsetning markaðsleyfis:
Framleiðslustaður fyrir losun lotu:
- Intervet International GmbH
Ábyrgt yfirvald:
- Federal Agency For Medicines And Health Products
Markaðsleyfisnúmer:
- BE-V179304
Dagsetning á breytingu stöðu:
Til að tilkynna upplýsingar um aukaverkanir vegna dýralyfja vinsamlegast farið á www.adrreports.eu/vet
Skjöl
Samantekt á eiginleikum lyfs
Þetta skjal er ekki til á þessu tungumáli (íslenska). Þú getur fundið það á öðru tungumáli hér að neðan.
Fylgiseðill
Þetta skjal er ekki til á þessu tungumáli (íslenska). Þú getur fundið það á öðru tungumáli hér að neðan.
Áletranir
Þetta skjal er ekki til á þessu tungumáli (íslenska). Þú getur fundið það á öðru tungumáli hér að neðan.
