Salmabic emulsija injekcijām vistām
Salmabic emulsija injekcijām vistām
Not authorised
- Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT B3, Inactivated
- Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT C8, Inactivated
- Salmonella enterica, subsp. enterica, serovar Typhimurium, strain PT 2(4+), Inactivated
Product identification
Medicine name:
Salmabic emulsija injekcijām vistām
Active substance:
- Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT B3, Inactivated
- Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT C8, Inactivated
- Salmonella enterica, subsp. enterica, serovar Typhimurium, strain PT 2(4+), Inactivated
Target species:
-
Chicken (layer hen)
-
Chicken (for reproduction)
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT B3, Inactivated100000000.00Colony forming unit1.00unit(s)
-
Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT C8, Inactivated100000000.00Colony forming unit1.00unit(s)
-
Salmonella enterica, subsp. enterica, serovar Typhimurium, strain PT 2(4+), Inactivated100000000.00Colony forming unit1.00unit(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Chicken (layer hen)
-
Chicken (for reproduction)
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Latvia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Abic Polska Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Abic Polska Sp. z o.o.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/11/0018
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Latvian (PDF)
Published on: 25/03/2024
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