PRIMUN SALMONELLA E
PRIMUN SALMONELLA E
Authorised
- Salmonella enterica, subsp. enterica, serovar Enteritidis, Live
Product identification
Medicine name:
PRIMUN SALMONELLA E
PRIMUN SALMONELLA E LYOPHILISAT POUR ADMINISTRATION DANS L'EAU DE BOISSON POUR POULETS
Active substance:
- Salmonella enterica, subsp. enterica, serovar Enteritidis, Live
Target species:
-
Chicken (pullet for egg production, future layer)
-
Future breeder pullet
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Salmonella enterica, subsp. enterica, serovar Enteritidis, Live600000000.00Colony forming unit1.00Dose
Pharmaceutical form:
-
Lyophilisate for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Chicken (pullet for egg production, future layer)
-
Meat and offalno withdrawal periodMeat and offal: 21 days after 1st, 2nd and 3rd vaccination. 14 days after 4th vaccination; Eggs: Zero days after 4th vaccination.
-
Eggsno withdrawal periodMeat and offal: 21 days after 1st, 2nd and 3rd vaccination. 14 days after 4th vaccination; Eggs: Zero days after 4th vaccination.
-
- Future breeder pullet
-
Meat and offalno withdrawal periodMeat and offal: 21 days after 1st, 2nd and 3rd vaccination. 14 days after 4th vaccination; Eggs: Zero days after 4th vaccination.
-
Eggsno withdrawal periodMeat and offal: 21 days after 1st, 2nd and 3rd vaccination. 14 days after 4th vaccination; Eggs: Zero days after 4th vaccination.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AE01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- cardboard box containing 10 vials (20 ml) of 2.000 doses
- cardboard box containing 10 vials (20 ml) of 1.000 doses
- cardboard box containing 1 vial (20 ml) of 2.000 doses
- cardboard box containing 1 vial (20 ml) of 1.000 doses
- Cardboard box containing 10 vials (20 ml) of 4000 doses
- Cardboard box containing 1 vial (20 ml) of 4000 doses
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Laboratorios Calier S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Calier S.A.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/8799020 9/2023
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0218/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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