NOBILIS MA 5 + CLONE 30 liofilizat pentru suspensie oculo-nazală sau pentru administrare în apa de băut pentru găini
NOBILIS MA 5 + CLONE 30 liofilizat pentru suspensie oculo-nazală sau pentru administrare în apa de băut pentru găini
Authorised
- Newcastle disease virus, strain Clone 30, Inactivated
- Infectious bronchitis virus, type Massachusetts, strain Ma5, Live
Product identification
Medicine name:
NOBILIS MA 5 + CLONE 30 liofilizat pentru suspensie oculo-nazală sau pentru administrare în apa de băut pentru găini
Active substance:
- Newcastle disease virus, strain Clone 30, Inactivated
- Infectious bronchitis virus, type Massachusetts, strain Ma5, Live
Target species:
-
Chicken (chick)
-
Chicken
Route of administration:
-
Oculonasal use
-
In drinking water use
Product details
Active substance and strength:
-
Newcastle disease virus, strain Clone 30, Inactivated6.00/log 10 50% embryo lethal dose1.00Dose
-
Infectious bronchitis virus, type Massachusetts, strain Ma5, Live3.00/log 10 50% embryo infective dose1.00Dose
Pharmaceutical form:
-
Lyophilisate for oculonasal suspension/use in drinking water
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD06
- QI01AD07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Romania
Available in:
-
Romania
Package description:
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
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:
- 120015
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Romanian (PDF)
Published on: 17/12/2025