Veterinary Medicines

Fevaxyn Quatrifel injektionsvæske, suspension

Authorised
  • Chlamydia felis, strain Cello, Inactivated
  • Feline calicivirus, strain 255, Inactivated
  • Feline rhinotracheitis virus, strain 605, Inactivated
  • Feline panleucopenia virus, strain CU4, Inactivated
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Product identification

Medicine name:
Fevaxyn Quatrifel injektionsvæske, suspension
Fevaxyn Quatrifel injektionsvæske, suspension
Active substance:
  • Chlamydia felis, strain Cello, Inactivated
  • Feline calicivirus, strain 255, Inactivated
  • Feline rhinotracheitis virus, strain 605, Inactivated
  • Feline panleucopenia virus, strain CU4, Inactivated
Target species:
  • Cat
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Chlamydia felis, strain Cello, Inactivated
    1.69
    relative potency
    /
    1.00
    millilitre(s)
  • Feline calicivirus, strain 255, Inactivated
    1.25
    relative potency
    /
    1.00
    millilitre(s)
  • Feline rhinotracheitis virus, strain 605, Inactivated
    1.39
    relative potency
    /
    1.00
    millilitre(s)
  • Feline panleucopenia virus, strain CU4, Inactivated
    8.50
    relative potency
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cat
  • Subcutaneous use
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI06AL02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Zoetis Animal Health ApS
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 14839
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Danish (PDF)
Published on: 29/06/2023
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