AviPro ND C131 Lyophilisate for suspension
AviPro ND C131 Lyophilisate for suspension
Authorised
- Newcastle disease virus, strain Clone 13-1, Live
Product identification
Medicine name:
AviPro ND C131 Lyophilisate for suspension
AviPro ND C131 lyofilizát na suspenziu pre kurčatá a morky
Active substance:
- Newcastle disease virus, strain Clone 13-1, Live
Target species:
-
Turkey
-
Chicken
Route of administration:
-
In drinking water use
-
Topical
-
Ocular use
Product details
Active substance and strength:
-
Newcastle disease virus, strain Clone 13-1, Live15848900.0050% Embryo Infective Dose1.00Dose
Pharmaceutical form:
-
Lyophilisate for oculonasal suspension/use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Turkey
-
Meat and offal0day
-
Egg0day
-
-
Chicken
-
Meat and offal0day
-
Egg0day
-
-
-
Topical
-
Chicken
-
Meat and offal0day
-
Egg0day
-
-
-
Ocular use
-
Chicken
-
Meat and offal0day
-
Egg0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- (ID8): 1 Box with 10 Bottle (Glass) with 5000 Dose (50000 Dose)
- (ID7): 1 Box with 1 Bottle (Glass) with 5000 Dose (5000 Dose)
- (ID11): 1 Box with 1 Bottle (Glass) with 2000 Dose (2000 Dose)
- (ID12): 1 Box with 10 Bottle (Glass) with 2000 Dose (20000 Dose)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Lohmann Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Lohmann Animal Health GmbH
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/064/MR/07-S
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0239/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Estonia
-
France
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 29/01/2024
Slovak (PDF)
Published on: 26/05/2023
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