PARVOKAN
PARVOKAN
Authorised
- Derzsy's disease virus, strain H, Live
- Muscovy duck parvovirus, strain GM, Inactivated
Product identification
Medicine name:
PARVOKAN
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, Live2.50log10 tissue culture infective dose 501.00Dose
-
Muscovy duck parvovirus, strain GM, Inactivated1.50log10 serum neutralising unit(s)1.00Dose
Pharmaceutical form:
-
Lyophilisate and suspension for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Duck
-
All relevant tissues0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01BH01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription except for some pack sizes
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- Box of one 1,500-dose bottle of suspension and three 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 ten 1,500-dose bottles of suspension and thirty 500-dose bottles of freeze-dried pellet
- Box of one 500-dose bottle of suspension and one 500-dose bottle 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 France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- National Veterinary Medicines Agency
Authorisation number:
- FR/V/5823169 2/2002
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0144/001
Concerned member states:
-
Germany
-
Italy
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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French (PDF)
Published on: 4/04/2022
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