Veterinary Medicines

Febrivac 3 plus vet. Injektionsvätska, suspension

Authorised
  • Pseudomonas aeruginosa, serotype 7/8, Inactivated
  • Pseudomonas aeruginosa, serotype 6, Inactivated
  • Pseudomonas aeruginosa, serotype 5, Inactivated
  • Mink enteritis virus, strain E-MINK F1, Inactivated
  • Clostridium botulinum, type C, toxoid
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Product identification

Medicine name:
Febrivac 3 plus vet. Injektionsvätska, suspension
Active substance:
  • Pseudomonas aeruginosa, serotype 7/8, Inactivated
  • Pseudomonas aeruginosa, serotype 6, Inactivated
  • Pseudomonas aeruginosa, serotype 5, Inactivated
  • Mink enteritis virus, strain E-MINK F1, Inactivated
  • Clostridium botulinum, type C, toxoid
Target species:
  • Mink
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Pseudomonas aeruginosa, serotype 7/8, Inactivated
    160.00
    unit(s)
    /
    1.00
    Dose
  • Pseudomonas aeruginosa, serotype 6, Inactivated
    160.00
    unit(s)
    /
    1.00
    Dose
  • Pseudomonas aeruginosa, serotype 5, Inactivated
    160.00
    unit(s)
    /
    1.00
    Dose
  • Mink enteritis virus, strain E-MINK F1, Inactivated
    4.00
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Clostridium botulinum, type C, toxoid
    0.50
    unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI20CL01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Sweden
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • CZ Vaccines S.A.U.
Marketing authorisation date:
Manufacturing sites for batch release:
  • IDT Biologika GmbH
Responsible authority:
  • Swedish Medical Products Agency
Authorisation number:
  • 11785
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 15/01/2025
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 15/01/2025
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