Veterinary Medicines

BOVIVAX LSD-N, lyophilisate and solvent for suspension for injection for cattle

Authorised
  • Lumpy skin disease virus, strain Neethling, Live
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Product identification

Medicine name:
BOVIVAX LSD-N, лиофилизат и дилуент за инжекционна суспензия за говеда
BOVIVAX LSD-N, lyophilisate and solvent for suspension for injection for cattle
Active substance:
  • Lumpy skin disease virus, strain Neethling, Live
Target species:
  • Cattle
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Lumpy skin disease virus, strain Neethling, Live
    3.50
    log10 (50% tissue culture infectious dose)/dose
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AU
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 (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Huvepharma EOOD
Marketing authorisation date:
Manufacturing sites for batch release:
  • Huvepharma EOOD
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-3322
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Bulgarian (PDF)
Published on: 20/08/2025
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Package Leaflet

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Bulgarian (PDF)
Published on: 20/08/2025
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Labelling

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Bulgarian (PDF)
Published on: 20/08/2025
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