Nobilis Salenvac T
Nobilis Salenvac T
Not authorised
- Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT4, Inactivated
- Salmonella enterica, subsp. enterica, serovar Typhimurium, strain DT104, Inactivated
Product identification
Medicine name:
Nobilis Salenvac T
Active substance:
- Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT4, Inactivated
- Salmonella enterica, subsp. enterica, serovar Typhimurium, strain DT104, Inactivated
Target species:
-
Chicken
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT4, Inactivated1.00/relative potency0.50millilitre(s)
-
Salmonella enterica, subsp. enterica, serovar Typhimurium, strain DT104, Inactivated1.00/relative potency0.50millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Chicken
-
Meat and offal0day
-
Egg0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Luxembourg
Package description:
- Cardboard box containing a 500 ml (1000 doses) low density polyethylene multi-dose bottle closed with an aluminium ring on top of a rubber stopper
- Cardboard box containing a 250 ml (500 doses) low density polyethylene multi-dose bottle closed with an aluminium ring on top of a rubber stopper
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Ministere De La Sante Division De La Pharmacie Et Des Medicaments
Authorisation number:
- V 817/04/02/0784
Date of authorisation status change:
Reference member state:
-
Italy
Procedure number:
- IT/V/0137/001
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: 16/02/2022