AviPro THYMOVAC Lyophilisate for use in drinking water
AviPro THYMOVAC Lyophilisate for use in drinking water
Authorised
- Chicken anaemia virus, strain CUX-1, Live
Product identification
Medicine name:
AviPro THYMOVAC Lyophilisate for use in drinking water
Avipro Thymovac Lyofilisaat voor gebruik in drinkwater
Avipro Thymovac Lyophilisat pour administration dans l'eau de boisson
Avipro Thymovac Lyophilisat zum Eingeben über das Trinkwasser
Active substance:
- Chicken anaemia virus, strain CUX-1, Live
Target species:
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Chicken anaemia virus, strain CUX-1, Live31622.00/50% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Lyophilisate for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken
-
Meat and offalno withdrawal periodwithdrawal period is 0 days
-
Eggno withdrawal periodwithdrawal period is 0 days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- (ID10): 1 Box with 10 Bottle (Glass) with 10000 Dose (100000 Dose)
- (ID9): 1 Box with 1 Bottle (Glass) with 10000 Dose (10000 Dose)
- (ID8): 1 Box with 10 Bottle (Glass) with 5000 Dose (50000 Dose)
- (ID7): 1 Box with 1 Bottle (Glass) with 5000 Dose (5000 Dose)
- (ID6): 1 Box with 10 Bottle (Glass) with 2500 Dose (25000 Dose)
- (ID5): 1 Box with 1 Bottle (Glass) with 2500 Dose (2500 Dose)
- (ID1): 1 Box with 1 Bottle (Glass) with 500 Dose (500 Dose)
- (ID2): 1 Box with 10 Bottle (Glass) with 500 Dose (5000 Dose)
- (ID4): 1 Box with 10 Bottle (Glass) with 1000 Dose (10000 Dose)
- (ID3): 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:
- Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Lohmann Animal Health GmbH
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V345362
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0247/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Combined File of all Documents
English (PDF)
Download Published on: 5/11/2024
Labelling
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