AviPro SALMONELLA DUO Lyophilisate for suspension
AviPro SALMONELLA DUO Lyophilisate for suspension
Authorised
- Salmonella enterica, subsp. enterica, serovar Enteritidis, strain Sm24/Rif12/Ssq, Live
- Salmonella enterica, subsp. enterica, serovar Typhimurium, strain Nal2/Rif9/Rtt, Live
Product identification
Medicine name:
AviPro SALMONELLA DUO Lyophilisate for suspension
AVIPRO SALMONELLA DUO
Active substance:
- Salmonella enterica, subsp. enterica, serovar Enteritidis, strain Sm24/Rif12/Ssq, Live
- Salmonella enterica, subsp. enterica, serovar Typhimurium, strain Nal2/Rif9/Rtt, Live
Target species:
-
Turkey
-
Chicken (for reproduction)
-
Duck
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Salmonella enterica, subsp. enterica, serovar Enteritidis, strain Sm24/Rif12/Ssq, Live600000000.00Colony forming unit1.00Dose
-
Salmonella enterica, subsp. enterica, serovar Typhimurium, strain Nal2/Rif9/Rtt, Live600000000.00Colony forming unit1.00Dose
Pharmaceutical form:
-
Lyophilisate for use in drinking water
Withdrawal period by route of administration:
-
In drinking water/milk use
- Turkey
-
Meat and offal70day70 days after first vaccination, 49 days after further vaccination
-
- Chicken (for reproduction)
-
Meat and offal21day
-
Egg21day
-
- Duck
-
Meat and offal21day
-
Egg21day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AE01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Available in:
-
France
Package description:
- (ID4): 1 Box with 10 Vials (Glass) with 2000 vaccine doses (20000 vaccine doses)
- (ID3): 1 Box with 10 Vials (Glass) with 1000 vaccine doses (10000 vaccine doses)
- (ID2): 1 Box with 1 Vial (Glass) with 2000 vaccine doses (2000 vaccine doses)
- (ID1): 1 Box with 1 Vial (Glass) with 1000 vaccine doses (1000 vaccine doses)
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:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/1117434 7/2011
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0249/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
France
-
Greece
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 2/03/2022
French (PDF)
Published on: 7/04/2022
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