Nobilis MS Live, lyophilisate for oculonasal suspension for chickens
Nobilis MS Live, lyophilisate for oculonasal suspension for chickens
Not authorised
- Mycoplasma synoviae, strain MS1, Live
Product identification
Medicine name:
Nobilis MS Live, lyophilisate for oculonasal suspension for chickens
Nobilis MS Live, Lyofilizát pro okulonazální suspenzi
Active substance:
- Mycoplasma synoviae, strain MS1, Live
Target species:
-
Chicken
-
Chicken (for reproduction)
Route of administration:
-
Oculonasal use
Product details
Active substance and strength:
-
Mycoplasma synoviae, strain MS1, Live100.00million colony forming units1.00Dose
Pharmaceutical form:
-
Lyophilisate for oculonasal suspension
Withdrawal period by route of administration:
-
Oculonasal use
- Chicken
-
Egg0day
-
Meat and offal0day
-
- Chicken (for reproduction)
-
Egg0day
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AE03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Czechia
Package description:
- (ID6): 1 Box with 10 Bottle (Glass) with 2000 Dose (20000 Dose)
- (ID5): 1 Box with 10 Bottle (Glass) with 1000 Dose (10000 Dose)
- (ID4): 1 Box with 10 Bottle (Glass) with 500 Dose (5000 Dose)
- (ID3): 1 Box with 1 Bottle (Glass) with 2000 Dose (2000 Dose)
- (ID2): 1 Box with 1 Bottle (Glass) with 1000 Dose (1000 Dose)
- (ID1): 1 Box with 1 Bottle (Glass) with 500 Dose (500 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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/009/14-C
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0260/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 28/01/2022
Czech (PDF)
Published on: 25/10/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 25/10/2022
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 25/10/2022
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