Salmoporc, lyophilisate and solvent for suspension for injection for pigs
Salmoporc, lyophilisate and solvent for suspension for injection for pigs
Authorised
- Salmonella enterica, subsp. enterica, serovar Typhimurium, Live
Product identification
Medicine name:
Salmoporc, lyophilisate and solvent for suspension for injection for pigs
Salmoporc, liofilizzato e solvente per sospensione iniettabile per suini
Active substance:
- Salmonella enterica, subsp. enterica, serovar Typhimurium, Live
Target species:
-
Pig
Route of administration:
-
Oral use
-
Subcutaneous use
Product details
Active substance and strength:
-
Salmonella enterica, subsp. enterica, serovar Typhimurium, Live8.00log10 colony forming unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Lyophilisate for suspension for injection
Withdrawal period by route of administration:
-
Oral use
-
Pig
-
Meat and offal6weeksix weeks after the second vaccination
-
-
-
Subcutaneous use
-
Pig
-
Meat and offal6weeksix weeks after the second vaccination
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AE02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Package description:
- Cardboard box containing 1 vial with 20 doses (1 dose = 1 ml) lyophilised vaccine
- 1 vial with 20 ml solvent
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Similar biological application (Article 13(4) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ceva Salute Animale S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva-Phylaxia Veterinary Biologicals Co. Ltd.
- IDT Biologika GmbH
Responsible authority:
- Ministry Of Health
Authorisation number:
- 105228
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0247/001
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Hungary
-
Ireland
-
Italy
-
Portugal
-
Romania
-
Slovakia
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Italian (PDF)
Published on: 26/09/2023
Updated on: 27/09/2023
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