NOBILIS MA 5 + CLONE 30
NOBILIS MA 5 + CLONE 30
Authorised
- Avian infectious bronchitis virus, type Massachusetts, strain Ma5, Live
- Newcastle disease virus, strain Clone 30, Live
Product identification
Medicine name:
NOBILIS MA 5 + CLONE 30
Active substance:
- Avian infectious bronchitis virus, type Massachusetts, strain Ma5, Live
- Newcastle disease virus, strain Clone 30, Live
Target species:
-
Chicken (one day-old chick)
Route of administration:
-
Nebulisation use
-
Oral use
-
Oculonasal use
Product details
Active substance and strength:
-
Avian infectious bronchitis virus, type Massachusetts, strain Ma5, Live3.00log 10 50% embryo infective dose1.00unit(s)
-
Newcastle disease virus, strain Clone 30, Live6.00log 10 50% embryo infective dose1.00unit(s)
Pharmaceutical form:
-
Lyophilisate for suspension
Withdrawal period by route of administration:
-
Nebulisation use
- Chicken (one day-old chick)
-
All relevant tissues0day
-
-
Oral use
- Chicken (one day-old chick)
-
All relevant tissues0day
-
-
Oculonasal use
- Chicken (one day-old chick)
-
All relevant tissues0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
- Available only in French
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/0323807 5/2000
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
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 4/04/2022
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