Veterinary Medicines

HuveGuard Duck RA

Authorised
  • Riemerella anatipestifer, serotype 5, strain SB1905, Live
  • Riemerella anatipestifer, serotype 2, strain SB1902, Live
  • Riemerella anatipestifer, serotype 1, strain SB1901, Live
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Product identification

Medicine name:
HuveGuard Duck RA
Active substance:
  • Riemerella anatipestifer, serotype 5, strain SB1905, Live
  • Riemerella anatipestifer, serotype 2, strain SB1902, Live
  • Riemerella anatipestifer, serotype 1, strain SB1901, Live
Target species:
  • Duck
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Riemerella anatipestifer, serotype 5, strain SB1905, Live
  • Riemerella anatipestifer, serotype 2, strain SB1902, Live
  • Riemerella anatipestifer, serotype 1, strain SB1901, Live
Pharmaceutical form:
  • Lyophilisate for oral suspension
Withdrawal period by route of administration:
  • In drinking water use
    • Duck
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AE
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 - new active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Huvepharma EOOD
Marketing authorisation date:
Manufacturing sites for batch release:
  • Biovet AD
  • Biovet AD
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-3185
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Bulgarian (PDF)
Published on: 16/10/2025
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Package Leaflet

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Bulgarian (PDF)
Published on: 16/10/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 16/10/2025
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