Veterinary Medicines

CEVAC LANDAVAX SC

Not authorised
  • Pasteurella multocida, serovar A3, strain P-1059, Inactivated
  • Pasteurella multocida, serovar A1, strain X-73, Inactivated
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Product identification

Medicine name:
CEVAC LANDAVAX SC
СЕВАК ЛАНДАВАКС SC
Active substance:
  • Pasteurella multocida, serovar A3, strain P-1059, Inactivated
  • Pasteurella multocida, serovar A1, strain X-73, Inactivated
Target species:
  • Duck
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Pasteurella multocida, serovar A3, strain P-1059, Inactivated
    65.00
    Percentage protective dose
    /
    1.00
    Dose
  • Pasteurella multocida, serovar A1, strain X-73, Inactivated
    80.00
    Percentage protective dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Duck
      • All relevant tissues
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01BB
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Bulgaria
Package description:
  • Box of 1 vial of 50 ml containing 100 doses
  • Box of 5 vial of 50 ml containing 100 doses
  • Vial of 500 ml containing 1000 doses
  • Box of 1 vial of 500 ml containing 1000 doses
  • Box of 5 vial of 500 ml containing 1000 doses
  • Vial of 50 ml containing 100 doses

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Ceva Animal Health Bulgaria EOOD
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva-Phylaxia Veterinary Biologicals Co. Ltd.
Responsible authority:
  • Bulgarian Agency For Food Safety
Authorisation number:
  • 0022-1744
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0238/001
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