Avipro IB H 120 lyofilisat til suspension
Avipro IB H 120 lyofilisat til suspension
Not authorised
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
Product identification
Medicine name:
Avipro IB H 120 lyofilisat til suspension
Avipro IB H 120 lyofilisat til suspension
Active substance:
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
- Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
Target species:
-
Poultry
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Avian infectious bronchitis virus, type Massachusetts, strain H120, Live1000.00/Embryo Infective Dose1.00Dose
-
Avian infectious bronchitis virus, type Massachusetts, strain H120, Live1000.00/Embryo Infective Dose1.00Dose
-
Avian infectious bronchitis virus, type Massachusetts, strain H120, Live1000.00/Embryo Infective Dose1.00Dose
-
Avian infectious bronchitis virus, type Massachusetts, strain H120, Live1000.00/Embryo Infective Dose1.00Dose
Pharmaceutical form:
-
Lyophilisate for suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Denmark
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Lohmann Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Lohmann Animal Health GmbH
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 06686
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
Danish (PDF)
Published on: 29/06/2023