Veterinary Medicines

SALMOPAST

Authorised
  • Pasteurella multocida, Serotype D, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Dublin, Inactivated
  • Pasteurella multocida, Serotype A, Inactivated
  • Mannheimia haemolytica, Inactivated
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Product identification

Medicine name:
SALMOPAST
Active substance:
  • Pasteurella multocida, Serotype D, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Dublin, Inactivated
  • Pasteurella multocida, Serotype A, Inactivated
  • Mannheimia haemolytica, Inactivated
Target species:
  • Cattle
  • Sheep
  • Goat
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Pasteurella multocida, Serotype D, Inactivated
    0.60
    enzyme-linked immunosorbent assay unit
    /
    1.00
    millilitre(s)
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, Inactivated
    1.50
    slow agglutination test unit(s)
    /
    1.00
    millilitre(s)
  • Salmonella enterica, subsp. enterica, serovar Dublin, Inactivated
    1.50
    slow agglutination test unit(s)
    /
    1.00
    millilitre(s)
  • Pasteurella multocida, Serotype A, Inactivated
    0.60
    enzyme-linked immunosorbent assay unit
    /
    1.00
    millilitre(s)
  • Mannheimia haemolytica, Inactivated
    0.60
    enzyme-linked immunosorbent assay unit
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • All relevant tissues
        0
        day
    • Sheep
      • All relevant tissues
        0
        day
    • Goat
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AB
  • QI03AB
  • QI04AB
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/8588182 8/1981
Date of authorisation status change:

Documents

Summary of Product Characteristics

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French (PDF)
Published on: 4/04/2022
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