GALLIVAC IB88 NEO EFFERVESCENT TABLET FOR OCULONASAL SUSPENSION
GALLIVAC IB88 NEO EFFERVESCENT TABLET FOR OCULONASAL SUSPENSION
Authorised
- Avian infectious bronchitis virus, type 793/B, strain CR88121, Live
Product identification
Medicine name:
GALLIVAC IB88 NEO EFFERVESCENT TABLET FOR OCULONASAL SUSPENSION
GALLIVAC IB88 NEO Brausetablette zur Herstellung einer Suspension zur oculonasalen Anwendung für Hühner
Active substance:
- Avian infectious bronchitis virus, type 793/B, strain CR88121, Live
Target species:
-
Chicken (broiler)
Route of administration:
-
Oculonasal use
Product details
Active substance and strength:
-
Avian infectious bronchitis virus, type 793/B, strain CR88121, Live4.00log 10 50% embryo infective dose1.00unit(s)
Pharmaceutical form:
-
Effervescent tablet
Withdrawal period by route of administration:
-
Oculonasal use
-
Chicken (broiler)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
Package description:
- Carton box of 1 blister of 10 tablets of 1 000 doses
- Carton box of 10 blisters of 10 tablets of 2 000 doses
- Carton box of 10 blisters of 10 tablets of 1 000 doses
- Carton box of 1 blister of 10 tablets of 2 000 doses
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 841196
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0450/001
Concerned member states:
-
Austria
-
Bulgaria
-
Croatia
-
Cyprus
-
Denmark
-
Finland
-
Greece
-
Iceland
-
Slovenia
-
Sweden
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 5/10/2022
Updated on: 14/08/2024
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 5/10/2022
Updated on: 14/08/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 5/10/2022
Updated on: 14/08/2024
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