HATCHPAK IB H120 NEO EFFERVESCENT TABLET FOR OCULONASAL SUSPENSION FOR CHICKENS
HATCHPAK IB H120 NEO EFFERVESCENT TABLET FOR OCULONASAL SUSPENSION FOR CHICKENS
Authorised
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
Product identification
Medicine name:
HATCHPAK IB H120 NEO EFFERVESCENT TABLET FOR OCULONASAL SUSPENSION FOR CHICKENS
HATCHPAK IB H120 freyðitafla fyrir dreifu til eimgjafar
Active substance:
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
Target species:
-
Chicken (one day-old chick)
Route of administration:
-
Oculonasal use
Product details
Active substance and strength:
-
Avian infectious bronchitis virus, type Massachusetts, strain H120, Live3.7050% Embryo Infective Dose1.00Dose
Pharmaceutical form:
-
Effervescent tablet
Withdrawal period by route of administration:
-
Oculonasal use
-
Chicken (one day-old chick)
-
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:
-
Iceland
Package description:
- Box of 1 blister of 10 tablets of 1,000 doses
- Box of 10 blisters of 10 tablets of 2,000 doses
- Box of 10 blisters of 10 tablets of 1,000 doses
- Box of 1 blister of 10 tablets of 2,000 doses
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Icelandic Medicines Agency
Authorisation number:
- IS/2/22/004/01
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0171/002
Concerned member states:
-
Belgium
-
Cyprus
-
Denmark
-
Finland
-
Germany
-
Greece
-
Iceland
-
Ireland
-
Italy
-
Netherlands
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
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.
Icelandic (PDF)
Published on: 20/06/2022
Updated on: 21/06/2022
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Icelandic (PDF)
Published on: 20/06/2022
Updated on: 21/06/2022
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