ORNIBUR Intermediate, Lyofilizát pro perorální a intrakonjunktivální použití.
ORNIBUR Intermediate, Lyofilizát pro perorální a intrakonjunktivální použití.
Authorised
- Infectious bursal disease virus, strain OP-3, Live
Product identification
Medicine name:
ORNIBUR Intermediate, Lyofilizát pro perorální a intrakonjunktivální použití.
Active substance:
- Infectious bursal disease virus, strain OP-3, Live
Target species:
-
Chicken
Route of administration:
-
In drinking water use
-
Ocular use
Product details
Active substance and strength:
-
Infectious bursal disease virus, strain OP-3, Live5.30log10 tissue culture infective dose 501.00Dose
Pharmaceutical form:
-
Lyophilisate for suspension
Withdrawal period by route of administration:
-
In drinking water use
- Chicken
-
Meat and offal0day
-
Egg0day
-
-
Ocular use
- Chicken
-
Meat and offal0day
-
Egg0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Package description:
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
- Available only in Czech
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:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicines
Authorisation number:
- 97/539/97-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: 26/10/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
How useful was this page?: