Veterinary Medicine Information website

Nobilis Reo Inac Emulsie voor injectie

Authorised
  • Avian reovirus, strain 1733, Inactivated
  • Avian reovirus, strain 2408, Inactivated
Download as PDF

Product identification

Medicine name:
Nobilis Reo Inac Emulsie voor injectie
Active substance:
  • Avian reovirus, strain 1733, Inactivated
  • Avian reovirus, strain 2408, Inactivated
Target species:
  • Chicken (for reproduction)
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Avian reovirus, strain 1733, Inactivated
    7.40
    enzyme-linked immunosorbent assay unit
    /
    0.50
    millilitre(s)
  • Avian reovirus, strain 2408, Inactivated
    7.40
    enzyme-linked immunosorbent assay unit
    /
    0.50
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Chicken (for reproduction)
      • Meat and offal
        0
        day
      • Egg
        0
        day
  • Subcutaneous use
    • Chicken (for reproduction)
      • Meat and offal
        0
        day
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • Nobilis Reo Inac 1 glass Vial with 1000 doses of Emulsion for injection
  • Nobilis Reo Inac 1 glass Vial with 500 doses of Emulsion for injection
  • Nobilis Reo Inac 1 PET Vial with 1000 doses of Emulsion for injection
  • Nobilis Reo Inac 1 PET Vial with 500 doses of Emulsion 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:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
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.
French (PDF)
Published on: 27/11/2025
Download
German (PDF)
Published on: 18/08/2025
Download
Dutch (PDF)
Published on: 18/08/2025
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 27/11/2025
Download
German (PDF)
Published on: 27/11/2025
Download
Dutch (PDF)
Published on: 27/11/2025
Download

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 27/11/2025
Download
Dutch (PDF)
Published on: 27/11/2025
Download