Overview

The marketing authorisation for this product has been withdrawn at the request of the marketing authorisation holder.

български (BG) (357.86 KB - PDF)

View

español (ES) (179.31 KB - PDF)

View

čeština (CS) (299.7 KB - PDF)

View

dansk (DA) (178.64 KB - PDF)

View

Deutsch (DE) (179.71 KB - PDF)

View

eesti keel (ET) (177.41 KB - PDF)

View

ελληνικά (EL) (363.86 KB - PDF)

View

français (FR) (179.1 KB - PDF)

View

italiano (IT) (180.25 KB - PDF)

View

latviešu valoda (LV) (304.16 KB - PDF)

View

lietuvių kalba (LT) (291.76 KB - PDF)

View

magyar (HU) (294.63 KB - PDF)

View

Malti (MT) (335.4 KB - PDF)

View

Nederlands (NL) (180.88 KB - PDF)

View

polski (PL) (309.91 KB - PDF)

View

português (PT) (180.78 KB - PDF)

View

română (RO) (285.47 KB - PDF)

View

slovenčina (SK) (297.9 KB - PDF)

View

slovenščina (SL) (289.13 KB - PDF)

View

Suomi (FI) (177.62 KB - PDF)

View

svenska (SV) (178.85 KB - PDF)

View

Product information

български (BG) (368.8 KB - PDF)

View

español (ES) (194.49 KB - PDF)

View

čeština (CS) (312.35 KB - PDF)

View

dansk (DA) (194.66 KB - PDF)

View

Deutsch (DE) (604.68 KB - PDF)

View

eesti keel (ET) (241.29 KB - PDF)

View

ελληνικά (EL) (369.72 KB - PDF)

View

français (FR) (192.68 KB - PDF)

View

italiano (IT) (194.62 KB - PDF)

View

latviešu valoda (LV) (343.7 KB - PDF)

View

lietuvių kalba (LT) (293.31 KB - PDF)

View

magyar (HU) (308.5 KB - PDF)

View

Malti (MT) (324.39 KB - PDF)

View

Nederlands (NL) (192.8 KB - PDF)

View

polski (PL) (337.03 KB - PDF)

View

português (PT) (241.72 KB - PDF)

View

română (RO) (296.25 KB - PDF)

View

slovenčina (SK) (316.44 KB - PDF)

View

slovenščina (SL) (299.37 KB - PDF)

View

Suomi (FI) (196.75 KB - PDF)

View

svenska (SV) (194.57 KB - PDF)

View

Latest procedure affecting product information: R/0005

29/08/2022

български (BG) (240.59 KB - PDF)

View

español (ES) (159.57 KB - PDF)

View

čeština (CS) (235.61 KB - PDF)

View

dansk (DA) (159.42 KB - PDF)

View

Deutsch (DE) (159.37 KB - PDF)

View

eesti keel (ET) (159.2 KB - PDF)

View

ελληνικά (EL) (82.3 KB - PDF)

View

français (FR) (159.37 KB - PDF)

View

italiano (IT) (159.39 KB - PDF)

View

latviešu valoda (LV) (234.13 KB - PDF)

View

lietuvių kalba (LT) (227.96 KB - PDF)

View

magyar (HU) (234.71 KB - PDF)

View

Malti (MT) (238.27 KB - PDF)

View

Nederlands (NL) (159.27 KB - PDF)

View

polski (PL) (234.03 KB - PDF)

View

português (PT) (159.39 KB - PDF)

View

română (RO) (224.27 KB - PDF)

View

slovenčina (SK) (234.38 KB - PDF)

View

slovenščina (SL) (230.29 KB - PDF)

View

Suomi (FI) (159.17 KB - PDF)

View

svenska (SV) (159.85 KB - PDF)

View

Product details

Name of medicine
Nobilis OR Inac
Active substance
inactivated whole cell suspension of Ornithobacterium rhinotracheale serotype A, strain B3263/91
International non-proprietary name (INN) or common name
adjuvanted inactivated vaccine against Ornithobacterium rhinotracheale serotype A
Species
Chicken
Anatomical therapeutic chemical veterinary (ATCvet) code
QI01AB07

Pharmacotherapeutic group

Immunologicals for aves

Therapeutic indication

For passive immunisation of broilers induced by active immunisation of female broiler breeders to reduce infection with Ornithobacterium rhinotracheale serotype A when this agent is involved.

Under field conditions passive immunity is transferred during lay for 43 weeks after the last vaccination of broiler breeders, resulting in a duration of passive immunity in broilers of at least 14 days after hatching.

Authorisation details

EMA product number
EMEA/V/C/000062
Marketing authorisation holder
Intervet International BV

Intervet International B.V.
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands

Marketing authorisation issued
24/01/2003
Revision
7

Assessment history

This page was last updated on

Share this page