Veterinary Medicines

GALLIMUNE 407 ND+IB+EDS+ART, emulzija za injekciju, za kokoši

Authorised
  • Turkey rhinotracheitis virus, strain VCO3, Inactivated
  • Eggdrop syndrome-1976 virus, strain V127, Inactivated
  • Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
  • Newcastle disease virus, strain Ulster 2C, Inactivated
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Product identification

Medicine name:
GALLIMUNE 407 ND+IB+EDS+ART, emulzija za injekciju, za kokoši
Active substance:
  • Turkey rhinotracheitis virus, strain VCO3, Inactivated
  • Eggdrop syndrome-1976 virus, strain V127, Inactivated
  • Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
  • Newcastle disease virus, strain Ulster 2C, Inactivated
Target species:
  • Chicken (layer hen)
  • Chicken (for reproduction)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Turkey rhinotracheitis virus, strain VCO3, Inactivated
    0.76
    log 10 optical density 50
    /
    0.30
    millilitre(s)
  • Eggdrop syndrome-1976 virus, strain V127, Inactivated
    180.00
    haemagglutination inhibiting unit(s)
    /
    0.30
    millilitre(s)
  • Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
    18.00
    haemagglutination inhibiting unit(s)
    /
    0.30
    millilitre(s)
  • Newcastle disease virus, strain Ulster 2C, Inactivated
    50.00
    50% Protective Dose
    /
    0.30
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Chicken (layer hen)
    • Chicken (for reproduction)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AA18
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Croatia
Available in:
  • Croatia
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:
  • Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/15-01/371
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Croatian (PDF)
Published on: 23/05/2024
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