KETEXX 100 MG/ML SOLUTION FOR INJECTION
KETEXX 100 MG/ML SOLUTION FOR INJECTION
Pooblaščeno
- Ketamine hydrochloride
Identifikacija zdravila
Ime zdravila:
Ketexx, 100 mg/ml, injekcinis tirpalas
KETEXX 100 MG/ML SOLUTION FOR INJECTION
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
-
Intravenska uporaba
-
Intraperitonealna uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English115.30milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Raztopina za injiciranje
Withdrawal period by route of administration:
-
intramuskularna uporaba
- govedo
-
Meat and offal1day
-
Milk0day
-
- Rat
- Mouse
- Hamster
- Guinea pig
- Rabbit (exclusively kept as pet)
-
All relevant tissuesno withdrawal periodNot authorised for use in rabbits for human consumption.
-
- Cat
- Horse
-
Meat and offal1day
-
Milk0day
-
- Dog
-
Intravenska uporaba
- govedo
-
Meat and offal1day
-
Milk0day
-
- Rat
- Mouse
- Hamster
- Guinea pig
- Rabbit (exclusively kept as pet)
-
All relevant tissuesno withdrawal periodNot authorised for use in rabbits for human consumption.
-
- Cat
- Horse
-
Meat and offal1day
-
Milk0day
-
- Sheep
-
Meat and offal1day
-
Milk0day
-
- Goat (adult female)
-
Meat and offal1day
-
Milk0day
-
- Dog
-
Intraperitonealna uporaba
- Rabbit (exclusively kept as pet)
-
All relevant tissuesno withdrawal periodNot authorised for use in rabbits for human consumption.
-
- Rat
- Mouse
- Hamster
- Guinea pig
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QN01AX03
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Alfasan Nederland B.V.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Alfasan Nederland B.V.
Pristojni organ:
- State Food And Veterinary Service
Številka dovoljenja :
- LT/2/22/2716/001-009
Datum spremembe statusa dovoljenja:
Številka postopka:
- FR/V/0435/001
Zadevne države članice:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
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Lithuanian (PDF)
Objavljeno na: 17/10/2023
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