NOBILIS REO S 1133 LYOPHILISAT ET SOLVANT POUR SUSPENSION INJECTABLE POUR POULES
NOBILIS REO S 1133 LYOPHILISAT ET SOLVANT POUR SUSPENSION INJECTABLE POUR POULES
Authorised
- Avian reovirus, strain S1133, Live
Product identification
Medicine name:
NOBILIS REO S 1133 LYOPHILISAT ET SOLVANT POUR SUSPENSION INJECTABLE POUR POULES
Active substance:
- Avian reovirus, strain S1133, Live
Target species:
-
Chicken (layer hen)
-
Chicken (one day-old chick)
-
Chicken (for reproduction)
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Avian reovirus, strain S1133, Live3.10/log10 50% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Chicken (layer hen)
-
All relevant tissues0day
-
-
Chicken (one day-old chick)
-
All relevant tissues0day
-
-
Chicken (for reproduction)
-
All relevant tissues0day
-
-
-
Subcutaneous use
-
Chicken (layer hen)
-
All relevant tissues0day
-
-
Chicken (one day-old chick)
-
All relevant tissues0day
-
-
Chicken (for reproduction)
-
All relevant tissues0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD10
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
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/2936167 4/1989
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: 23/04/2025
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 23/04/2025