Veterinary Medicine Information website

Nobilis Reo+IB+G+ND

Authorised
  • Avian reovirus, strains 1733 and 2408, Inactivated
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
  • Infectious bursal disease virus, strain D78, Inactivated
  • Newcastle disease virus, Inactivated
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Product identification

Medicine name:
Nobilis Reo+IB+G+ND
Active substance:
  • Avian reovirus, strains 1733 and 2408, Inactivated
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
  • Infectious bursal disease virus, strain D78, Inactivated
  • Newcastle disease virus, Inactivated
Target species:
  • Chicken (for reproduction)
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Avian reovirus, strains 1733 and 2408, Inactivated
    7.40
    log2 enzyme-linked immunosorbent assay unit(s)
    /
    1.00
    dose
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
    6.00
    log2 haemagglutination inhibiting unit(s)
    /
    1.00
    dose
  • Infectious bursal disease virus, strain D78, Inactivated
    14.50
    log2 virus neutralising unit(s)
    /
    1.00
    dose
  • Newcastle disease virus, Inactivated
    50.00
    50% Protective Dose
    /
    1.00
    dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Chicken (for reproduction)
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Chicken (for reproduction)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AA16
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Estonia
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:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • State Agency Of Medicines
Authorisation number:
  • 1338
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.
Estonian (PDF)
Published on: 29/06/2023
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