Ovilis Enzovax Lyophilisate and solvent for suspension for injection for sheep
Ovilis Enzovax Lyophilisate and solvent for suspension for injection for sheep
Not authorised
- Chlamydia abortus, strain 1B (thermosensitive), Live
Product identification
Medicine name:
Ovilis Enzovax Lyophilisate and solvent for suspension for injection for sheep
OVILIS ENZOVAX, Injekční suspenze
Active substance:
- Chlamydia abortus, strain 1B (thermosensitive), Live
Target species:
-
Sheep
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Chlamydia abortus, strain 1B (thermosensitive), Live100000.00/Fluorescent Focus Forming Unit1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Sheep
-
Meat and offal7day
-
-
-
Intramuscular use
-
Sheep
-
Meat and offal7day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI04AE01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Czechia
Package description:
- (ID3): 1 Box with 10 Box with (1 Bottle (Glass) with 1 Dose and 1 Bottle (Glass) with 2 millilitre(s)) (10 Dose, 20 millilitre(s))
- (ID7): 1 Box with 100 Box with (1 Bottle (Glass) with 1 Dose and 1 Bottle (Glass) with 2 millilitre(s)) (100 Dose, 200 millilitre(s))
- (ID6): 1 Box with 50 Box with (1 Bottle (Glass) with 1 Dose and 1 Bottle (Glass) with 2 millilitre(s)) (50 Dose, 100 millilitre(s))
- (ID4): 1 Box with 20 Box with (1 Bottle (Glass) with 1 Dose and 1 Bottle (Glass) with 2 millilitre(s)) (20 Dose, 40 millilitre(s))
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:
- 97/024/08-C
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0246/001
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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