ICTHIOVAC-STR ESTREPTOCOCOSIS RODABALLO Suspension for injection
ICTHIOVAC-STR ESTREPTOCOCOSIS RODABALLO Suspension for injection
Not authorised
- Streptococcus parauberis, strain AZ-12.1, Inactivated
- Streptococcus parauberis, strain RA-99.1, Inactivated
Product identification
Medicine name:
ICTHIOVAC-STR ESTREPTOCOCOSIS RODABALLO Suspension for injection
ICTHIOVAC-STR ESTREPTOCOCCOSIOS ΚΑΛΚΑΝΙ ενέσιμο διάλυμα για καλκάνι
Active substance:
- Streptococcus parauberis, strain AZ-12.1, Inactivated
- Streptococcus parauberis, strain RA-99.1, Inactivated
Target species:
-
Turbot
Route of administration:
-
Intraperitoneal use
Product details
Active substance and strength:
-
Streptococcus parauberis, strain AZ-12.1, Inactivated75.00/Relative Percentage Survival0.10millilitre(s)
-
Streptococcus parauberis, strain RA-99.1, Inactivated75.00/Relative Percentage Survival0.10millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intraperitoneal use
-
Turbot
-
Meat0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI10D
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Greece
Package description:
- bottle of 500 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Hipra S.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 88496/09/08-12-2010/K-0158301
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0109/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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