XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
Odobreno
- Xylazine hydrochloride
Identifikacija proizvoda
Naziv lijeka:
XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
Djelatna tvar:
- Dostupan samo u engleski
Ciljne vrste:
Put aplikacije:
-
Intramuskularno
-
Intravenski
Pojedinosti o proizvodu
Djelatna tvar i jačina:
-
Dostupan samo u engleski583.00/miligram1.00mililitar
Farmaceutski oblik:
-
Liofilizat i otapalo za suspenziju za injekciju
Karencija prema putu aplikacije:
-
Intramuskularno
-
Cattle
-
Meat and offal3day
-
Milk36sat3 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
-
-
-
Intravenski
-
Cattle
-
Meat and offal3day
-
Milk36sat3 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-terapijsko-kemijska veterinarska (ATKvet) oznaka:
- QN05CM92
Status odobrenja:
-
Važeće
Odobreno u:
- Dostupan samo u španjolski češki njemački estonski engleski francuski talijanski nizozemski portugalski slovački švedski islandski Norwegian
Dodatne informacije
Vrsta prava:
-
Marketing Authorisation
Pravna osnova za odobrenje proizvoda:
Nositelj odobrenja za stavljanje u promet:
- Vetservis s.r.o.
Datum odobrenja za stavljanje u promet:
Mjesta proizvodnje za otpuštanje serije:
- Bioveta a.s.
Nadležno tijelo:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Broj odobrenja:
- 96/059/13-S
Datum promjene statusa odobrenja:
Za izvješća o sumnjama na nuspojave veterinarskog lijeka molimo vas otiđite na www.adrreports.eu/vet
Dokumenti
Combined File of all Documents
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slovački (PDF)
Objavljeno na: 7/03/2023
