Nobilis IB+ND+EDS vakcina A.U.V.
Nobilis IB+ND+EDS vakcina A.U.V.
Authorised
- Newcastle disease virus, strain Clone 30, Inactivated
- Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Egg drop syndrome '76 virus, strain BC14, Inactivated
Product identification
Medicine name:
Nobilis IB+ND+EDS vakcina A.U.V.
Active substance:
- Newcastle disease virus, strain Clone 30, Inactivated
- Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Egg drop syndrome '76 virus, strain BC14, Inactivated
Target species:
-
Chicken (hen)
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Newcastle disease virus, strain Clone 30, Inactivated4.00log2 haemagglutination inhibiting unit(s)1.00unit(s)/dose
-
Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated6.00log2 haemagglutination inhibiting unit(s)1.00unit(s)/dose
-
Egg drop syndrome '76 virus, strain BC14, Inactivated6.50log2 haemagglutination inhibiting unit(s)1.00unit(s)/dose
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Chicken (hen)
-
Meat and offal0day
-
Meat and offal0day
-
-
Subcutaneous use
- Chicken (hen)
-
Meat and offal0day
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AA13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Package description:
- Available only in Hungarian
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 International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Directorate Of Veterinary Medicinal Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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