Veterinary Medicines

Fohlenlähme-Mischserum

Authorised
  • Immunoglobulins against Escherichia coli, Salmonella dublin, Salmonella enteritidis, Salmonella typhimurium, Salmonella rostock, Salmonella abortusequi, Streptococcus pneumoniae, Streptococcus equi subsp. zooepidemicus, Equine
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Product identification

Medicine name:
Fohlenlähme-Mischserum
Active substance:
  • Immunoglobulins against Escherichia coli, Salmonella dublin, Salmonella enteritidis, Salmonella typhimurium, Salmonella rostock, Salmonella abortusequi, Streptococcus pneumoniae, Streptococcus equi subsp. zooepidemicus, Equine
Target species:
  • Horse
  • Horse (foal)
  • Horse (suckling foal)
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Immunoglobulins against Escherichia coli, Salmonella dublin, Salmonella enteritidis, Salmonella typhimurium, Salmonella rostock, Salmonella abortusequi, Streptococcus pneumoniae, Streptococcus equi subsp. zooepidemicus, Equine
    16.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Horse (foal)
      • Meat and offal
        0
        day
    • Horse (suckling foal)
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI05AM03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Package description:

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:
  • Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Marketing authorisation date:
Manufacturing sites for batch release:
  • Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Responsible authority:
  • Paul-Ehrlich-Institut
Authorisation number:
  • A269/79
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 27/02/2024
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 27/02/2024
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