Veterinary Medicines

PARVOKAN LYOPHILISATE AND SUSPENSION FOR SUSPENSION FOR INJECTION

Authorised
  • Derzsy's disease virus, strain H, Live
  • Muscovy duck parvovirus, strain GM, Inactivated
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Product identification

Medicine name:
PARVOKAN LYOPHILISATE AND SUSPENSION FOR SUSPENSION FOR INJECTION
PARVOKAN
Active substance:
  • Derzsy's disease virus, strain H, Live
  • Muscovy duck parvovirus, strain GM, Inactivated
Target species:
  • Duck
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Derzsy's disease virus, strain H, Live
    2.50
    log10 50% cell culture infectious dose
    /
    1.00
    Dose
  • Muscovy duck parvovirus, strain GM, Inactivated
    1.50
    log10 serum neutralising unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and suspension for suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Duck
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01BH01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:
  • Box of one 500-dose bottle of suspension and one 500-dose bottle of freeze-dried pellet
  • Box of ten 1,500-dose bottles of suspension and thirty 500-dose bottles of freeze-dried pellet
  • Box of ten 500-dose bottles of suspension and ten 500-dose bottles of freeze-dried pellet
  • Box of one 1,500-dose bottle of suspension and three 500-dose bottles of freeze-dried pellet

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Boehringer Ingelheim Animal Health Italia S.p.A. In Breve Boehringer Ingelheim Ah It S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 104060
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0144/001
Concerned member states:
  • Germany
  • Italy

Documents

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Published on: 1/07/2022
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