MULTIVAC PSG инжекционна емулсия за свине
MULTIVAC PSG инжекционна емулсия за свине
Authorised
- Haemophilus parasuis, strain IL-1-DEP, Inactivated
- Pasteurella multocida, strain 9, Inactivated
- Pasteurella multocida, strain 1231, Inactivated
- Salmonella enterica, subsp. enterica, serovar Typhimurium, strain 371, Inactivated
- Salmonella enterica, subsp. enterica, serovar Choleraesuis, strain 370, Inactivated
Product identification
Medicine name:
MULTIVAC PSG инжекционна емулсия за свине
Active substance:
- Haemophilus parasuis, strain IL-1-DEP, Inactivated
- Pasteurella multocida, strain 9, Inactivated
- Pasteurella multocida, strain 1231, Inactivated
- Salmonella enterica, subsp. enterica, serovar Typhimurium, strain 371, Inactivated
- Salmonella enterica, subsp. enterica, serovar Choleraesuis, strain 370, Inactivated
Target species:
-
Pig
Route of administration:
-
Injection
Product details
Active substance and strength:
-
Haemophilus parasuis, strain IL-1-DEP, Inactivated2.00/billion organisms1.00Dose
-
Pasteurella multocida, strain 9, Inactivated2.00/billion organisms1.00Dose
-
Pasteurella multocida, strain 1231, Inactivated2.00/billion organisms1.00Dose
-
Salmonella enterica, subsp. enterica, serovar Typhimurium, strain 371, Inactivated2.00/billion organisms1.00Dose
-
Salmonella enterica, subsp. enterica, serovar Choleraesuis, strain 370, Inactivated2.00/billion organisms1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Mintech Co EOOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Mintech Co EOOD
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2926
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
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 3/05/2023
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 11/06/2022