Veterinary Medicines

Vaccine against Anthrax, suspension for injection for horses, donkeys, mules, camels, cattle, buffaloes, sheep, goats and pigs

Authorised
  • Bacillus anthracis, strain Sterne 34F2, Live
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Product identification

Medicine name:
Ваксина против антракс, инжекционна суспензия за коне, магарета, мулета, камили, говеда, биволи, овце, кози и свине
Vaccine against Anthrax, suspension for injection for horses, donkeys, mules, camels, cattle, buffaloes, sheep, goats and pigs
Active substance:
  • Bacillus anthracis, strain Sterne 34F2, Live
Target species:
  • Horse
  • Donkey
  • Camel
  • Cattle
  • Buffalo
  • Sheep
  • Goat
  • Pig
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Bacillus anthracis, strain Sterne 34F2, Live
    7.00
    log10 colour changing units
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Horse
      • Meat and offal
        15
        day
    • Cattle
      • Meat and offal
        15
        day
    • Buffalo
      • Meat and offal
        15
        day
    • Sheep
      • Meat
        15
        LD100 concentration for mice after i.m. injection after 5 days
    • Goat
      • Meat and offal
        15
        day
    • Pig
      • Meat and offal
        15
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AE04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Bulgaria
Package description:

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:
  • Sopharma AD
Marketing authorisation date:
Manufacturing sites for batch release:
  • Sopharma AD
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-2173
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.
Bulgarian (PDF)
Published on: 29/12/2025
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Package Leaflet

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Bulgarian (PDF)
Published on: 29/12/2025
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Labelling

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Bulgarian (PDF)
Published on: 29/12/2025
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