Veterinary Medicine Information website

Nobilis RT+IBmulti+G+ND Emulsion for injection (water-in-oil)

Authorised
  • Newcastle disease virus, strain Clone 30, Inactivated
  • Infectious bursal disease virus, strain D78, Inactivated
  • Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated
  • Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
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Product identification

Medicine name:
Nobilis RT+IBmulti+G+ND Emulsion for injection (water-in-oil)
Active substance:
  • Newcastle disease virus, strain Clone 30, Inactivated
  • Infectious bursal disease virus, strain D78, Inactivated
  • Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated
  • Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
Target species:
  • Chicken
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Newcastle disease virus, strain Clone 30, Inactivated
    50.00
    50% Protective Dose
    /
    0.50
    millilitre(s)
  • Infectious bursal disease virus, strain D78, Inactivated
    14.50
    log2 virus neutralising unit(s)
    /
    0.50
    millilitre(s)
  • Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated
    9.50
    log2 enzyme-linked immunosorbent assay unit(s)
    /
    0.50
    millilitre(s)
  • Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
    4.00
    log2 virus neutralising unit(s)
    /
    0.50
    millilitre(s)
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
    5.50
    log2 virus neutralising unit(s)
    /
    0.50
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Chicken
      • Meat and offal
        0
        day
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Available in:
  • Netherlands
Package description:
  • (ID2) 500 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 500 millilitre(s)
  • (ID1) 250 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 250 millilitre(s)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 9707
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0212/001
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • France
  • Greece
  • Ireland
  • Italy
  • Luxembourg
  • Netherlands
  • Portugal
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 30/01/2024
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