Lactetrol Solution injectable
Lactetrol Solution injectable
Ima dovoljenje za promet
- Potassium chloride
- Sodium chloride
- Sodium lactate
- Calcium chloride dihydrate
- Magnesium chloride hexahydrate
Informacije o zdravilu
Ime zdravila:
Lactetrol Solution injectable
Lactetrol Injektionslösung
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
Subkutana uporaba
-
Intravenska uporaba
-
Intraperitonealna uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English0.37/milligram(s)1.00millilitre(s)
-
Na voljo samo v English5.76/milligram(s)1.00millilitre(s)
-
Na voljo samo v English10.08/milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.37/milligram(s)1.00millilitre(s)
-
Na voljo samo v English0.20/milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za infundiranje
Karenca glede na pot uporabe:
-
Subkutana uporaba
-
govedo
-
Meat and offal, milkno withdrawal period
-
-
Horse
-
Meat and offal, milkno withdrawal period
-
-
Sheep
-
Meat and offal, milkno withdrawal period
-
-
Goat
-
Meat and offal, milkno withdrawal period
-
-
Pig
-
Meat and offalno withdrawal period
-
-
-
Intravenska uporaba
-
govedo
-
Meat and offal, milkno withdrawal period
-
-
Horse
-
Meat and offal, milkno withdrawal period
-
-
Sheep
-
Meat and offal, milkno withdrawal period
-
-
Goat
-
Meat and offal, milkno withdrawal period
-
-
Pig
-
Meat and offalno withdrawal period
-
-
-
Intraperitonealna uporaba
-
govedo
-
Meat and offal, milkno withdrawal period
-
-
Horse
-
Meat and offal, milkno withdrawal period
-
-
Sheep
-
Meat and offal, milkno withdrawal period
-
-
Goat
-
Meat and offal, milkno withdrawal period
-
-
Pig
-
Meat and offalno withdrawal period
-
-
Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):
- QB05XA30
Pravni status za dobavo/izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja za promet z zdravilom:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Dechra Veterinary Products
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
- Eurovet Animal Health B.V.
Pristojni organ:
- Ministere De La Sante Division De La Pharmacie Et Des Medicaments
Številka dovoljenja za promet z zdravilom:
- V 855/15/04/1443
Datum spremembe statusa dovoljenja za promet:
Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet
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Objavljeno na dan: 6/11/2023
Updated on: 7/11/2023