Nobilis ND Clone 30, liofilizatas suspensijai į akį ar šnervę ruošti / naudoti su geriamuoju vandeniu vištoms ir kalakutams
Nobilis ND Clone 30, liofilizatas suspensijai į akį ar šnervę ruošti / naudoti su geriamuoju vandeniu vištoms ir kalakutams
Authorised
- Newcastle disease virus, strain Clone 30, Live
Product identification
Medicine name:
Nobilis ND Clone 30, liofilizatas suspensijai į akį ar šnervę ruošti / naudoti su geriamuoju vandeniu vištoms ir kalakutams
Active substance:
- Newcastle disease virus, strain Clone 30, Live
Target species:
-
Chicken
-
Turkey
Route of administration:
-
Oculonasal use
-
Nebulisation use
-
In drinking water use
Product details
Active substance and strength:
-
Newcastle disease virus, strain Clone 30, Live6.00/log 10 50% embryo lethal dose1.00Dose
Pharmaceutical form:
-
Lyophilisate for oculonasal suspension/use in drinking water
Withdrawal period by route of administration:
-
Oculonasal use
-
Chicken
-
Meat and offal0day
-
-
Turkey
-
Meat and offal0day
-
-
-
Nebulisation use
-
Chicken
-
Meat and offal0day
-
-
Turkey
-
Meat and offal0day
-
-
-
In drinking water use
-
Chicken
-
Meat and offal0day
-
-
Turkey
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD06
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/95/0259/001-007
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
This document does not exist in this language (English). You can find it
in another language below.
Lithuanian (PDF)
Published on: 12/04/2023
RV0259.pdf
Lithuanian (PDF)
Download Published on: 22/06/2022