Veterinary Medicines

Deparvax

Authorised
  • Muscovy duck parvovirus, strain FM, Inactivated
  • Derzsy's disease virus, strain LB, Inactivated
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Product identification

Medicine name:
Deparvax
Deparvax, emulsja do wstrzykiwań dla kaczek piżmowych i gęsi
Active substance:
  • Muscovy duck parvovirus, strain FM, Inactivated
  • Derzsy's disease virus, strain LB, Inactivated
Target species:
  • Muscovy duck
  • Goose
Route of administration:
  • Subcutaneous use
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Muscovy duck parvovirus, strain FM, Inactivated
    7.70
    log2 virus neutralising unit(s)
    /
    0.20
    millilitre(s)
  • Derzsy's disease virus, strain LB, Inactivated
    7.90
    log2 virus neutralising unit(s)
    /
    0.20
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Muscovy duck
      • Meat and offal
        0
        day
  • Intramuscular use
    • Muscovy duck
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Goose
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01BA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Package description:
  • Available only in Polish
  • Available only in Polish
  • 100 ml, 250 dose, for breeder geese
  • 100ml, 500 dose for day-old or growing birds

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:
  • Ceva-Phylaxia Zrt.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva-Phylaxia Zrt.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 1727
Date of authorisation status change:
Reference member state:
  • Hungary
Procedure number:
  • HU/V/100/001
Concerned member states:
  • Poland

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 31/10/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 31/10/2025
Download