XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
Pooblaščeno
- Xylazine hydrochloride
Identifikacija zdravila
Ime zdravila:
XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
Učinkovina:
- Na voljo samo v English
Ciljne živalske vrste:
-
govedo
Pot uporabe:
-
intramuskularna uporaba
-
Intravenska uporaba
Podatki o zdravilu
Učinkovina / Jakost:
-
Na voljo samo v English583.00milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Liofilizat in vehikel za suspenzijo za injiciranje
Withdrawal period by route of administration:
-
intramuskularna uporaba
- govedo
-
Meat and offal3day
-
Milk36hour3 milkings
-
- Horse
-
All relevant tissuesno withdrawal periodDo not use in horses which meat and milk are intended for human consumption
-
- Red deer
-
All relevant tissuesno withdrawal periodDo not use in animals which meat is intended for human consumption
-
- Fallow deer
-
All relevant tissuesno withdrawal periodDo not use in animals which meat is intended for human consumption
-
- Roe deer
-
All relevant tissuesno withdrawal periodDo not use in animals which meat is intended for human consumption
-
-
Intravenska uporaba
- govedo
-
Meat and offal3day
-
Milk36hour3 milkings
-
- Horse
-
All relevant tissuesno withdrawal periodDo not use in horses which meat and milk are intended for human consumption
-
- Red deer
-
All relevant tissuesno withdrawal periodDo not use in animals which meat is intended for human consumption
-
- Fallow deer
-
All relevant tissuesno withdrawal periodDo not use in animals which meat is intended for human consumption
-
- Roe deer
-
All relevant tissuesno withdrawal periodDo not use in animals which meat is intended for human consumption
-
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
- QN05CM92
Pravni status za dobavo / izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja:
-
Valid
Dodatne informacije
Imetnik dovoljenja za promet z zdravilom:
- Vetservis s.r.o.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
- Bioveta a.s.
Pristojni organ:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Številka dovoljenja :
- 96/059/13-S
Datum spremembe statusa dovoljenja:
Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet
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Slovak (PDF)
Objavljeno na: 7/03/2023
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