Nobilis RT+IBmulti+G+ND emulsija injekcijām vistām
Nobilis RT+IBmulti+G+ND emulsija injekcijām vistām
Authorised
- Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
- Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated
- Infectious bursal disease virus, strain D78, Inactivated
- Newcastle disease virus, strain Clone 30, Inactivated
Product identification
Medicine name:
Nobilis RT+IBmulti+G+ND emulsija injekcijām vistām
Active substance:
- Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated
- Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated
- Infectious bursal disease virus, strain D78, Inactivated
- Newcastle disease virus, strain Clone 30, Inactivated
Target species:
-
Chicken (for reproduction)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated5.50/log2 virus neutralising unit(s)1.00unit(s)
-
Infectious bronchitis virus, type D274/D207, strain 249g, Inactivated4.00/log2 virus neutralising unit(s)1.00unit(s)
-
Turkey rhinotracheitis virus, strain BUT1#8544, Inactivated9.50/log2 enzyme-linked immunosorbent assay unit(s)1.00unit(s)
-
Infectious bursal disease virus, strain D78, Inactivated14.50/log2 virus neutralising unit(s)1.00unit(s)
-
Newcastle disease virus, strain Clone 30, Inactivated50.00/50% Protective Dose1.00unit(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Chicken (for reproduction)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Available in:
-
Latvia
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:
- Food And Veterinary Service
Authorisation number:
- V/NRP/03/1535
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 3/02/2026