Avipol IBD Każda dawka szczepionki zawiera: Żywy średnio atenuowany wirus zakaźnego zapalenia torby Fabrycjusza (IBD), szczep Winterfield 2512: nie mniej niż 102 EID50* i nie więcej niż 103 EID50* Liofilizat do podania w wodzie do picia
Avipol IBD Każda dawka szczepionki zawiera: Żywy średnio atenuowany wirus zakaźnego zapalenia torby Fabrycjusza (IBD), szczep Winterfield 2512: nie mniej niż 102 EID50* i nie więcej niż 103 EID50* Liofilizat do podania w wodzie do picia
Authorised
- Infectious bursal disease virus, strain Winterfield 2512 (intermediate plus), Inactivated
Product identification
Medicine name:
Avipol IBD Każda dawka szczepionki zawiera: Żywy średnio atenuowany wirus zakaźnego zapalenia torby Fabrycjusza (IBD), szczep Winterfield 2512: nie mniej niż 102 EID50* i nie więcej niż 103 EID50* Liofilizat do podania w wodzie do picia
Active substance:
- Infectious bursal disease virus, strain Winterfield 2512 (intermediate plus), Inactivated
Target species:
-
Chicken (hen)
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Infectious bursal disease virus, strain Winterfield 2512 (intermediate plus), Inactivated
Pharmaceutical form:
-
Lyophilisate for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken (hen)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 3406
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 27/11/2025
Summary of Product Characteristics
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in another language below.
Polish (PDF)
Published on: 27/11/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 27/11/2025