SG-VAC LIVE Źywe, liofilizowane komórki Salmonella enterica subsp. enterica serowar Gallinarum/pullorumatenuowany szczep SGP695AV, nie mniej niż 2 × 10^8 CFU i nie więcej niż 1 × 10^9 CFU Liofilizat do sporządzania zawiesiny doustnej
SG-VAC LIVE Źywe, liofilizowane komórki Salmonella enterica subsp. enterica serowar Gallinarum/pullorumatenuowany szczep SGP695AV, nie mniej niż 2 × 10^8 CFU i nie więcej niż 1 × 10^9 CFU Liofilizat do sporządzania zawiesiny doustnej
Authorised
- Salmonella enterica, subsp. enterica, serovar Gallinarum, strain SGP695AV, Live
Product identification
Medicine name:
SG-VAC LIVE Źywe, liofilizowane komórki Salmonella enterica subsp. enterica serowar Gallinarum/pullorumatenuowany szczep SGP695AV, nie mniej niż 2 × 10^8 CFU i nie więcej niż 1 × 10^9 CFU Liofilizat do sporządzania zawiesiny doustnej
Active substance:
- Salmonella enterica, subsp. enterica, serovar Gallinarum, strain SGP695AV, Live
Target species:
-
Chicken (hen)
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Salmonella enterica, subsp. enterica, serovar Gallinarum, strain SGP695AV, Live1000000000.00/Colony forming unit1.00Colony forming unit
Pharmaceutical form:
-
Lyophilisate for oral suspension
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken (hen)
-
All relevant tissues0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AE01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2577
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet