Norvax Compact PD Emulsion for Injection for Atlantic Salmon
Norvax Compact PD Emulsion for Injection for Atlantic Salmon
Not authorised
- Salmon pancreas disease virus, strain F93-125, Inactivated
Product identification
Medicine name:
Norvax compact PD emulsion for injection for Atlantic salmon
Norvax Compact PD Emulsion for Injection for Atlantic Salmon
Active substance:
- Salmon pancreas disease virus, strain F93-125, Inactivated
Target species:
-
Atlantic salmon
Route of administration:
-
Intraperitoneal use
Product details
Active substance and strength:
-
Salmon pancreas disease virus, strain F93-125, Inactivated50118700.00/50% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intraperitoneal use
-
Atlantic salmon
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI10AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Expired
Authorised in:
-
United Kingdom (Northern Ireland)
Package description:
- Bottles of polyethylene terephthalate (PET) closed with a rubber stopper and aluminium cap. Pack size: 250 ml (2,500 doses).
- Bottles of polyethylene terephthalate (PET) closed with a rubber stopper and aluminium cap. Pack size: 500 ml (5,000 doses).
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:
- MSD Animal Health UK Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- The Veterinary Medicines Directorate
Authorisation number:
- Vm 01708/3037
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0257/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet