Veterinary Medicines

ORNIVAC FC, Injekční emulze

Authorised
  • Pasteurella multocida, serotype A1, strain X-73, Inactivated
  • Pasteurella multocida, serotype A3, strain P-1059, Inactivated
  • Pasteurella multocida, serotype A4, strain P-1662, Inactivated
  • Pasteurella multocida, serotype A3x4, strain CU, Inactivated
Download as PDF

Product identification

Medicine name:
ORNIVAC FC, Injekční emulze
Active substance:
  • Pasteurella multocida, serotype A1, strain X-73, Inactivated
  • Pasteurella multocida, serotype A3, strain P-1059, Inactivated
  • Pasteurella multocida, serotype A4, strain P-1662, Inactivated
  • Pasteurella multocida, serotype A3x4, strain CU, Inactivated
Target species:
  • Chicken
  • Turkey
Route of administration:
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Pasteurella multocida, serotype A1, strain X-73, Inactivated
    1.00
    relative potency
    /
    1.00
    Dose
  • Pasteurella multocida, serotype A3, strain P-1059, Inactivated
    1.00
    relative potency
    /
    1.00
    Dose
  • Pasteurella multocida, serotype A4, strain P-1662, Inactivated
    1.00
    relative potency
    /
    1.00
    Dose
  • Pasteurella multocida, serotype A3x4, strain CU, Inactivated
    1.00
    relative potency
    /
    1.00
    Dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Chicken
      • Meat and offal
        0
        day
      • Egg
        0
        day
    • Turkey
      • Meat and offal
        0
        day
      • Egg
        0
        day
  • Intramuscular use
    • Chicken
      • Meat and offal
        0
        day
      • Egg
        0
        day
    • Turkey
      • Meat and offal
        0
        day
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - known active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/022/25-C
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 21/07/2025
Download

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 21/07/2025
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 21/07/2025
Download