XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
Ima dovoljenje za promet
- Xylazine hydrochloride
Informacije o zdravilu
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 English583.00/milligram(s)1.00millilitre(s)
Farmacevtska oblika:
-
Liofilizat in vehikel za suspenzijo za injiciranje
Karenca glede na pot uporabe:
-
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 klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):
- QN05CM92
Pravni status za dobavo/izdajo zdravila:
-
Zdravilo, ki se izdaja na veterinarski recept
Status dovoljenja za promet z zdravilom:
-
Valid
Dodatne informacije
Pravna podlaga za izdajo dovoljenja za promet z zdravilom:
Imetnik dovoljenja za promet z zdravilom:
- Vetservis s.r.o.
Datum dovoljenja za promet z zdravilom:
Proizvodna mesta, odgovorna za sproščanje serij:
- Bioveta a.s.
Pristojni organ:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Številka dovoljenja za promet z zdravilom:
- 96/059/13-S
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: 7/03/2023