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Nobilis RT + IB Multi + ND + EDS emulsja do wstrzykiwań dla kur

Authorised
  • Newcastle disease virus, strain Clone 30, Inactivated
  • Eggdrop syndrome-1976 virus, strain BC14, Inactivated
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
  • Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
  • Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated
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Product identification

Medicine name:
Nobilis RT + IB Multi + ND + EDS emulsja do wstrzykiwań dla kur
Active substance:
  • Newcastle disease virus, strain Clone 30, Inactivated
  • Eggdrop syndrome-1976 virus, strain BC14, Inactivated
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
  • Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
  • Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated
Target species:
  • Chicken (hen)
Route of administration:
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Newcastle disease virus, strain Clone 30, Inactivated
    50.00
    50% Protective Dose
    /
    1.00
    50% Protective Dose
  • Eggdrop syndrome-1976 virus, strain BC14, Inactivated
    1.00
    unknown
    /
    1.00
    unknown
  • Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
    1.00
    unknown
    /
    1.00
    unknown
  • Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
    1.00
    unknown
    /
    1.00
    unknown
  • Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated
    1.00
    unknown
    /
    1.00
    unknown
Pharmaceutical form:
  • Emulsion for injection/infusion
Withdrawal period by route of administration:
  • Subcutaneous use
    • Chicken (hen)
      • Meat and offal
        0
        day
  • Intramuscular use
    • Chicken (hen)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AA18
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Available in:
  • Poland
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.
  • Merck Sharp & Dohme Animal Health S.L.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 1118
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.
Polish (PDF)
Published on: 16/03/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 16/03/2022
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 15/11/2024
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