NOBILIS RT + IBmulti + ND + EDS
NOBILIS RT + IBmulti + ND + EDS
Authorised
- Egg drop syndrome '76 virus, strain V127, Inactivated
- Newcastle disease virus, strain Clone 30, Inactivated
- Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Avian infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
- Turkey rhinotracheitis virus, strain BUT1#8544, Live
Product identification
Medicine name:
NOBILIS RT + IBmulti + ND + EDS
Active substance:
- Egg drop syndrome '76 virus, strain V127, Inactivated
- Newcastle disease virus, strain Clone 30, Inactivated
- Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Avian infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
- Turkey rhinotracheitis virus, strain BUT1#8544, Live
Target species:
-
Chicken (for reproduction)
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Egg drop syndrome '76 virus, strain V127, Inactivated6.50log2 haemagglutination inhibiting unit(s)0.50millilitre(s)
-
Newcastle disease virus, strain Clone 30, Inactivated50.0050% Protective Dose0.50millilitre(s)
-
Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated5.50log2 virus neutralising unit(s)0.50millilitre(s)
-
Avian infectious bronchitis virus, type D274/D207, strain 249g, Inactivated4.00log2 virus neutralising unit(s)0.50millilitre(s)
-
Turkey rhinotracheitis virus, strain BUT1#8544, Live9.50log2 enzyme-linked immunosorbent assay unit(s)0.50millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Chicken (for reproduction)
-
Intramuscular use
- Chicken (for reproduction)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AA18
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Romania
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - 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:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 120265
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Romanian (PDF)
Published on: 2/04/2024
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