Veterinary Medicines

IZOVAC ND-EDS-IBD

Suspended
  • Newcastle disease virus, strain La Sota, Inactivated
  • Eggdrop syndrome-1976 virus, strain McFerran 127, Inactivated
  • Infectious bursal disease virus, strain Winterfield 2512 (intermediate plus), Inactivated
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Product identification

Medicine name:
IZOVAC ND-EDS-IBD
Active substance:
  • Newcastle disease virus, strain La Sota, Inactivated
  • Eggdrop syndrome-1976 virus, strain McFerran 127, Inactivated
  • Infectious bursal disease virus, strain Winterfield 2512 (intermediate plus), Inactivated
Target species:
  • Chicken (layer hen)
  • Chicken (pullet)
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Newcastle disease virus, strain La Sota, Inactivated
    50.00
    50% Protective Dose
    /
    250.00
    millilitre(s)
  • Eggdrop syndrome-1976 virus, strain McFerran 127, Inactivated
    7.00
    log2 haemagglutination inhibiting unit(s)
    /
    250.00
    millilitre(s)
  • Infectious bursal disease virus, strain Winterfield 2512 (intermediate plus), Inactivated
    9.00
    log2 haemagglutination inhibiting unit(s)
    /
    250.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Chicken (layer hen)
      • Meat and offal
        30
        day
    • Chicken (pullet)
      • Meat and offal
        30
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AA09
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Suspended
Authorised in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Izo S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Izo S.r.l.
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change: