NEMOVAC, lyofilizát pro přípravu orální suspenze, Lyofilizát pro orální suspenzi
NEMOVAC, lyofilizát pro přípravu orální suspenze, Lyofilizát pro orální suspenzi
Authorised
- Turkey rhinotracheitis virus, strain PL21, Live
Product identification
Medicine name:
NEMOVAC, lyofilizát pro přípravu orální suspenze, Lyofilizát pro orální suspenzi
Active substance:
- Turkey rhinotracheitis virus, strain PL21, Live
Target species:
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Turkey rhinotracheitis virus, strain PL21, Live4.00log10 cell culture infective dose 501.00Dose
Pharmaceutical form:
-
Lyophilisate for oral suspension
Withdrawal period by route of administration:
-
In drinking water use
- Chicken
-
Meat and offal0day
-
Egg0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
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:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/064/99-C
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.
Czech (PDF)
Published on: 22/06/2023
Package Leaflet
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in another language below.
Czech (PDF)
Published on: 22/06/2023
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 22/06/2023
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