Poulvac Bursa Plus Lyophilisate for suspension in drinking water
Poulvac Bursa Plus Lyophilisate for suspension in drinking water
Authorised
- Infectious bursal disease virus, strain V877, Live
Product identification
Medicine name:
Poulvac Bursa Plus Lyophilisate for suspension in drinking water
Poulvac Bursa Plus Lyofilisaat voor gebruik in drinkwater
Poulvac Bursa Plus Lyophilisat pour administration dans l'eau de boisson
Poulvac Bursa Plus Lyophilisat zum Eingeben über das Trinkwasser
Active substance:
- Infectious bursal disease virus, strain V877, Live
Target species:
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Infectious bursal disease virus, strain V877, Live2511.8950% Embryo Infective Dose1.00Dose
Pharmaceutical form:
-
Lyophilisate for suspension
Withdrawal period by route of administration:
-
In drinking water use
- Chicken
-
Egg0day
-
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:
-
Belgium
Package description:
- (ID6): 1 Box with 10 Bottle (Glass) with 5000 Dose (50000 Dose)
- (ID5): 1 Box with 10 Bottle (Glass) with 2000 Dose (20000 Dose)
- (ID4): 1 Box with 10 Bottle (Glass) with 1000 Dose (10000 Dose)
- (ID3): 1 Box with 1 Bottle (Glass) with 5000 Dose (5000 Dose)
- (ID2): 1 Box with 1 Bottle (Glass) with 2000 Dose (2000 Dose)
- (ID1): 1 Box with 1 Bottle (Glass) with 1000 Dose (1000 Dose)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
- FAMHP
Authorisation number:
- BE-V380895
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0278/001
Concerned member states:
-
Belgium
-
Greece
-
Ireland
-
Italy
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovenia
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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