Nobilis Reo + IB + G + ND emulsja do wstrzykiwań dla kur
Nobilis Reo + IB + G + ND emulsja do wstrzykiwań dla kur
Authorised
- Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Newcastle disease virus, strain Clone 30, Inactivated
- Infectious bursal disease virus, strain D78, Live
- Avian reovirus, strain 1733, Inactivated
Product identification
Medicine name:
Nobilis Reo + IB + G + ND emulsja do wstrzykiwań dla kur
Active substance:
- Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Newcastle disease virus, strain Clone 30, Inactivated
- Infectious bursal disease virus, strain D78, Live
- Avian reovirus, strain 1733, Inactivated
Target species:
-
Chicken (hen)
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
-
Newcastle disease virus, strain Clone 30, Inactivated50.0050% Protective Dose0.01millilitre(s)
-
Infectious bursal disease virus, strain D78, Live
-
Avian reovirus, strain 1733, Inactivated
Pharmaceutical form:
-
Emulsion for injection/infusion
Withdrawal period by route of administration:
-
Intramuscular use
- Chicken (hen)
-
Meat and offal0day
-
-
Subcutaneous use
- Chicken (hen)
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- Available only in Polish
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Merck Sharp & Dohme Animal Health S.L.
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0137
Date of authorisation status change:
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.
Polish (PDF)
Published on: 16/03/2022
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