Veterinary Medicines

Footvax, Injekční emulze

Authorised
  • Dichelobacter nodosus, serogroup I, Inactivated
  • Dichelobacter nodosus, serogroup H, Inactivated
  • Dichelobacter nodosus, serogroup G, Inactivated
  • Dichelobacter nodosus, serogroup F, Inactivated
  • Dichelobacter nodosus, serogroup E, Inactivated
  • Dichelobacter nodosus, serogroup C, Inactivated
  • Dichelobacter nodosus, serogroup D, Inactivated
  • Dichelobacter nodosus, serotype B2, Inactivated
  • Dichelobacter nodosus, serotype B1, Inactivated
  • Dichelobacter nodosus, serogroup A, Inactivated
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Product identification

Medicine name:
Footvax, Injekční emulze
Active substance:
  • Dichelobacter nodosus, serogroup I, Inactivated
  • Dichelobacter nodosus, serogroup H, Inactivated
  • Dichelobacter nodosus, serogroup G, Inactivated
  • Dichelobacter nodosus, serogroup F, Inactivated
  • Dichelobacter nodosus, serogroup E, Inactivated
  • Dichelobacter nodosus, serogroup C, Inactivated
  • Dichelobacter nodosus, serogroup D, Inactivated
  • Dichelobacter nodosus, serotype B2, Inactivated
  • Dichelobacter nodosus, serotype B1, Inactivated
  • Dichelobacter nodosus, serogroup A, Inactivated
Target species:
  • Sheep
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Dichelobacter nodosus, serogroup I, Inactivated
    500000000.00
    cells
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serogroup H, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serogroup G, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serogroup F, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serogroup E, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serogroup C, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serogroup D, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype B2, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype B1, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serogroup A, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI04AB03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Package description:

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:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/023/01-C
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 20/12/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 20/12/2023
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 20/12/2023
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