Veterinary Medicines

Fevaxyn Quatrifel Suspensie voor injectie

Not authorised
  • Felid herpesvirus 1, strain 605, Inactivated
  • Feline panleucopenia virus, strain CU4, Inactivated
  • Feline calicivirus, strain 255, Inactivated
  • Chlamydia felis, strain Cello, Inactivated
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Product identification

Medicine name:
Fevaxyn Quatrifel Suspensie voor injectie
Fevaxyn Quatrifel Suspension injectable
Fevaxyn Quatrifel Injektionssuspension
Active substance:
  • Felid herpesvirus 1, strain 605, Inactivated
  • Feline panleucopenia virus, strain CU4, Inactivated
  • Feline calicivirus, strain 255, Inactivated
  • Chlamydia felis, strain Cello, Inactivated
Target species:
  • Cat
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Felid herpesvirus 1, 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)
  • Feline calicivirus, strain 255, Inactivated
    1.26
    relative potency
    /
    1.00
    millilitre(s)
  • Chlamydia felis, strain Cello, Inactivated
    1.69
    relative potency
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cat
      • All relevant tissues
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI06AL01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Belgium
Package description:
  • Fevaxyn Quatrifel 10 Pre-filled syringes with 1 ml Suspension for injection

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:
  • Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V174912
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Dutch (PDF)
Published on: 22/03/2022
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French (PDF)
Published on: 22/03/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
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French (PDF)
Published on: 22/03/2022
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German (PDF)
Published on: 22/03/2022
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