Veterinary Medicines

Febrivac 3-Plus Zawiesina do wstrzykiwań

Authorised
  • Mink enteritis virus, strain E-MINK F1, Inactivated
  • Pseudomonas aeruginosa, serotype 5, strain EP3, Inactivated
  • Pseudomonas aeruginosa, serotype 6, strain EP2, Inactivated
  • Pseudomonas aeruginosa, serotype 7/8, strain EP1, Inactivated
  • Clostridium botulinum, type C, strain Stockholm, toxoid
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Product identification

Medicine name:
Febrivac 3-Plus Zawiesina do wstrzykiwań
Active substance:
  • Mink enteritis virus, strain E-MINK F1, Inactivated
  • Pseudomonas aeruginosa, serotype 5, strain EP3, Inactivated
  • Pseudomonas aeruginosa, serotype 6, strain EP2, Inactivated
  • Pseudomonas aeruginosa, serotype 7/8, strain EP1, Inactivated
  • Clostridium botulinum, type C, strain Stockholm, toxoid
Target species:
  • Mink
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Mink enteritis virus, strain E-MINK F1, Inactivated
  • Pseudomonas aeruginosa, serotype 5, strain EP3, Inactivated
  • Pseudomonas aeruginosa, serotype 6, strain EP2, Inactivated
  • Pseudomonas aeruginosa, serotype 7/8, strain EP1, Inactivated
  • Clostridium botulinum, type C, strain Stockholm, toxoid
    80.00
    percent
    /
    1.00
    percent
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Mink
      • All relevant tissues
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI20CL01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
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:
  • IDT Biologika GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • IDT Biologika GmbH
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 1262
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.
Polish (PDF)
Published on: 16/03/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 16/03/2022
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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.
Polish (PDF)
Published on: 15/11/2024
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