Nobilis AE + POX Liofilizzato e solvente per sospensione iniettabile per polli e tacchini
Nobilis AE + POX Liofilizzato e solvente per sospensione iniettabile per polli e tacchini
Authorised
- Avian encephalomyelitis virus, strain Calnek 1143, Live
- Fowlpox virus, strain GIBBS, Live
Product identification
Medicine name:
Nobilis AE + POX Liofilizzato e solvente per sospensione iniettabile per polli e tacchini
Nobilis AE + POX Liofilizzato e solvente per sospensione iniettabile per polli e tacchini
Active substance:
- Avian encephalomyelitis virus, strain Calnek 1143, Live
- Fowlpox virus, strain GIBBS, Live
Target species:
-
Chicken (for reproduction)
-
Chicken (pullet for egg production, future layer)
-
Turkey (for reproduction)
Route of administration:
-
Wing-web-stab use
Product details
Active substance and strength:
-
Avian encephalomyelitis virus, strain Calnek 1143, Live1.80log 10 50% embryo infective dose1.00Dose
-
Fowlpox virus, strain GIBBS, Live1.80log 10 50% embryo infective dose1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Wing-web-stab use
- Chicken (for reproduction)
-
Meat and offal0day
-
- Chicken (pullet for egg production, future layer)
-
Meat and offal0day
-
Egg0day
-
- Turkey (for reproduction)
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Package description:
- Available only in Italian
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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- MINSAL
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 20/04/2023
How useful was this page?: