Veterinary Medicines Information website

BIOSUIS Salm emulsion for injection for pigs

Not authorised
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Derby, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Infantis, Inactivated
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Product identification

Medicine name:
BIOSUIS Salm emulsion for injection for pigs
Active substance:
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Derby, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Infantis, Inactivated
Target species:
  • Pig (pregnant sow)
  • Pig (pregnant gilt)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, Inactivated
    1.00
    relative potency
    /
    1.00
    Dose
  • Salmonella enterica, subsp. enterica, serovar Derby, Inactivated
    1.00
    relative potency
    /
    1.00
    Dose
  • Salmonella enterica, subsp. enterica, serovar Infantis, Inactivated
    1.00
    relative potency
    /
    1.00
    Dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig (pregnant sow)
      • Meat and offal
        0
        day
    • Pig (pregnant gilt)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB14
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Slovakia
Package description:
  • Glass Vial 1 x 10.0 Dose
  • Plastic Vial 1 x 50.0 Dose
  • Plastic Vial 1 x 100.0 Dose
  • Glass Vial 10 x 10.0 Dose

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:
  • Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/032/DC/19-S
Date of authorisation status change:
Reference member state:
  • Czechia
Procedure number:
  • CZ/V/0151/001

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 2/03/2022
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Summary of Product Characteristics

English (PDF)
Published on: 14/03/2026
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Package Leaflet

English (PDF)
Published on: 14/03/2026
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Labelling

English (PDF)
Published on: 14/03/2026
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eu-puar-czv0151001-mr-biosuis_salm-en.pdf

English (PDF)
Published on: 14/03/2026
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