NOBILIS AE + POX, liofilizat și solvent pentru suspensie injectabilă
NOBILIS AE + POX, liofilizat și solvent pentru suspensie injectabilă
Authorised
- Avian encephalomyelitis virus, strain Calnek 1143, Live
- Fowlpox virus, strain GIBBS, Live
Product identification
Medicine name:
NOBILIS AE + POX, liofilizat și solvent pentru suspensie injectabilă
Active substance:
- Avian encephalomyelitis virus, strain Calnek 1143, Live
- Fowlpox virus, strain GIBBS, Live
Target species:
-
Chicken (hen)
-
Turkey (hen)
Route of administration:
-
Intradermal use
Product details
Active substance and strength:
-
Avian encephalomyelitis virus, strain Calnek 1143, Live1.80log 10 50% embryo infective dose0.01millilitre(s)
-
Fowlpox virus, strain GIBBS, Live1.80log 10 50% embryo infective dose0.01millilitre(s)
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intradermal use
- Chicken (hen)
-
Meat and offal0day
-
- Turkey (hen)
-
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:
-
Romania
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - 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:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 150250
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Romanian (PDF)
Published on: 23/11/2021
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