Veterinary Medicines Information website

MYXOREN lyofilizát a rozpúšťadlo na injekčnú suspenziu

Authorised
  • Myxoma virus, strain CAMP V-219, Live
  • Myxoma virus, strain CAMP V-219, Live
  • Myxoma virus, strain CAMP V-219, Live
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Product identification

Medicine name:
MYXOREN lyofilizát a rozpúšťadlo na injekčnú suspenziu
Active substance:
  • Myxoma virus, strain CAMP V-219, Live
  • Myxoma virus, strain CAMP V-219, Live
  • Myxoma virus, strain CAMP V-219, Live
Target species:
  • Rabbit
  • Rabbit
  • Rabbit
Route of administration:
  • Transdermal use
  • Intradermal use
  • Subcutaneous use

Product details

Active substance and strength:
  • Myxoma virus, strain CAMP V-219, Live
    2.60
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Myxoma virus, strain CAMP V-219, Live
    2.70
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Myxoma virus, strain CAMP V-219, Live
    3.30
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Transdermal use
    • Rabbit
      • All relevant tissues
        0
        day
  • Intradermal use
    • Rabbit
      • All relevant tissues
        0
        day
  • Subcutaneous use
    • Rabbit
      • Adipose tissue
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI08AD02
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 (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/191/91-S
Date of authorisation status change:

Documents

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Slovak (PDF)
Published on: 9/07/2025
Updated on: 13/03/2026
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