POULVAC POULINAC ND+IB M41+EDS EMULSION INJECTABLE POUR POULETS
POULVAC POULINAC ND+IB M41+EDS EMULSION INJECTABLE POUR POULETS
Authorised
- Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Newcastle disease virus, strain Ulster 2C, Inactivated
- Eggdrop syndrome-1976 virus, strain McFerran 127, Inactivated
Product identification
Medicine name:
POULVAC POULINAC ND+IB M41+EDS EMULSION INJECTABLE POUR POULETS
Active substance:
- Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Newcastle disease virus, strain Ulster 2C, Inactivated
- Eggdrop syndrome-1976 virus, strain McFerran 127, Inactivated
Target species:
-
Chicken (layer hen)
-
Chicken (for reproduction)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Infectious bronchitis virus, type Massachusetts, strain M41, Inactivated3.30/log10 ELISA unit1.00Dose
-
Newcastle disease virus, strain Ulster 2C, Inactivated24.00/antigen unit(s)1.00Dose
-
Eggdrop syndrome-1976 virus, strain McFerran 127, Inactivated9.20/log2 haemagglutination inhibiting unit(s)1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Chicken (layer hen)
-
All relevant tissues0day
-
-
Chicken (for reproduction)
-
All relevant tissues0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AA13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - known active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Zoetis France
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/1479875 9/2025
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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: 13/03/2026
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: 13/03/2026
fr-puar-700000188295-np-rpe919-fr.pdf
French (PDF)
Download Published on: 13/03/2026