AVINEW NEO EFFERVESCENT TABLET FOR CHICKENS AND TURKEYS
AVINEW NEO EFFERVESCENT TABLET FOR CHICKENS AND TURKEYS
Not authorised
- Newcastle disease virus, strain VG/GA, Live
Product identification
Medicine name:
AVINEW NEO EFFERVESCENT TABLET FOR CHICKENS AND TURKEYS
Avinew Neo Bruistablet
Avinew Neo Comprimé effervescent
Avinew Neo Brausetablette
Active substance:
- Newcastle disease virus, strain VG/GA, Live
Target species:
-
Chicken (layer hen)
-
Chicken (for reproduction)
-
Chicken (broiler)
-
Turkey
Route of administration:
-
Ocular use
-
Oral use
-
Oculonasal use
Product details
Active substance and strength:
-
Newcastle disease virus, strain VG/GA, Live5.50/log10 50% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Effervescent tablet
Withdrawal period by route of administration:
-
Ocular use
-
Chicken (layer hen)
-
All relevant tissues0day
-
-
Chicken (for reproduction)
-
All relevant tissues0day
-
-
Chicken (broiler)
-
All relevant tissues0day
-
-
-
Oral use
-
Chicken (layer hen)
-
All relevant tissues0day
-
-
Chicken (for reproduction)
-
All relevant tissues0day
-
-
Chicken (broiler)
-
All relevant tissues0day
-
-
-
Oculonasal use
-
Turkey
-
All relevant tissues0day
-
-
Chicken (for reproduction)
-
All relevant tissues0day
-
-
Chicken (broiler)
-
All relevant tissues0day
-
-
Chicken (layer hen)
-
All relevant tissues0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Box of 10 blisters of 10 tablets of 2,000 doses
- Box of 1 blister of 10 tablets of 1,000 doses
- Box of 1 blister of 10 tablets of 2,000 doses
- Box of 10 blisters of 10 tablets of 1,000 doses
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V483306
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0296/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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Summary of Product Characteristics
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