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NOBILIS RT+IBmulti+G+ND, injekcinė emulsija vištoms

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, injekcinė emulsija vištoms
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 (for reproduction)
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 (for reproduction)
      • Meat and offal
        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:
  • Lithuania
Available in:
  • Lithuania
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • State Food And Veterinary Service
Authorisation number:
  • LT/2/03/1555/001-002
Date of authorisation status change:

Documents

Combined File of all Documents

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Lithuanian (PDF)
Published on: 27/01/2026
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