T 61 Oplossing voor injectie
T 61 Oplossing voor injectie
Dopuszczony
- Mebezonium iodide
- Embutramide
- Tetracaine hydrochloride
Identyfikacja produktu
Nazwa leku:
T 61 Oplossing voor injectie
T 61 Solution injectable
T 61 Injektionslösung
Gatunki docelowe:
Droga podania:
-
Podanie do płuc
-
Podanie dosercowe
-
Podanie dożylne
Szczegóły produktu
Postać farmaceutyczna:
-
Roztwór do wstrzykiwań
Okres karencji w zależności od drogi podania:
-
Podanie do płuc
-
Dog
-
Meat and offalno 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
-
-
Cat
-
Meat and offalno 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
-
Meat and offalno 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
-
-
Ornamental bird
-
Meat and offalno 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
-
Meat and offalno 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
-
-
Pigeon
-
Meat and offalno 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
-
-
-
Podanie dosercowe
-
Dog
-
Meat and offalno 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
-
-
-
Podanie dożylne
-
Cattle
-
Meat and offalno 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
-
-
Horse
-
Meat and offalno 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
-
-
Dog
-
Meat and offalno 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
-
-
Kod klasyfikacji anatomiczno-terapeutyczno-chemicznej (ATCvet):
- QN51AX50
Status pozwolenia:
-
Valid
Opis opakowania:
- Dostępne wyłącznie w Angielski
Informacje dodatkowe
Podmiot odpowiedzialny:
- Intervet International B.V.
Data pozwolenia na dopuszczenie do obrotu:
Miejsca wytwarzania, gdzie następuje zwolnienie serii:
- Intervet International GmbH
Organ odpowiedzialny:
- Federal Agency For Medicines And Health Products
Numer pozwolenia:
- BE-V179304
Data zmiany statusu pozwolenia:
Zgłoszenia podejrzewanych działań niepożądanych: www.adrreports.eu/vet
Dokumenty
Charakterystyka produktu leczniczego
Ten dokument nie istnieje w tym języku (polski). Możesz go znaleźć w innym języku poniżej.
Ulotka dla pacjenta
Ten dokument nie istnieje w tym języku (polski). Możesz go znaleźć w innym języku poniżej.
oznakowanie opakowań
Ten dokument nie istnieje w tym języku (polski). Możesz go znaleźć w innym języku poniżej.
Jak przydatna była ta strona?: