Veterinary Medicine Information website

NOBILIS REO+IB+G+ND

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

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

Product details

Active substance and strength:
  • Water for injection
    1.00
    millilitre(s)
    /
    0.50
    millilitre(s)
  • Glycine
    5.00
    milligram(s)
    /
    0.50
    millilitre(s)
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
    6.00
    log2 haemagglutination inhibiting unit(s)
    /
    0.50
    millilitre(s)
  • Infectious bursal disease virus, strain D78, Inactivated
    12.50
    log2 virus neutralising unit(s)
    /
    0.50
    millilitre(s)
  • Avian reovirus, strains 1733 and 2408, Inactivated
    5.00
    log2 virus neutralising unit(s)
    /
    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
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AA16
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
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:
  • Merck Sharp & Dohme Animal Health S.L.
  • Intervet International B.V.
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

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Italian (PDF)
Published on: 2/02/2024
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