Veterinary Medicines

XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom

Authorised
  • Xylazine hydrochloride
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Product identification

Medicine name:
XYLASED 500 mg lyofilizát na prípravu injekčného roztoku s rozpúšťadlom
Active substance:
  • Xylazine hydrochloride
Target species:
  • Cattle
  • Horse
  • Red deer
  • Fallow deer
  • Roe deer
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Xylazine hydrochloride
    583.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        3
        day
      • Milk
        36
        hour
    • Horse
      • All relevant tissues
        no withdrawal period
    • Red deer
      • All relevant tissues
        no withdrawal period
    • Fallow deer
      • All relevant tissues
        no withdrawal period
    • Roe deer
      • All relevant tissues
        no withdrawal period
  • Intravenous use
    • Cattle
      • Meat and offal
        3
        day
      • Milk
        36
        hour
    • Horse
      • All relevant tissues
        no withdrawal period
    • Red deer
      • All relevant tissues
        no withdrawal period
    • Fallow deer
      • All relevant tissues
        no withdrawal period
    • Roe deer
      • All relevant tissues
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN05CM92
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Vetservis s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/059/13-S
Date of authorisation status change:

Documents

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Slovak (PDF)
Published on: 7/03/2023
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