OVAX CLAMIDIA, ενέσιμο εναιώρημα για πρόβατα
OVAX CLAMIDIA, ενέσιμο εναιώρημα για πρόβατα
Authorised
- Chlamydia abortus, Inactivated
Product identification
Medicine name:
OVAX CLAMIDIA, ενέσιμο εναιώρημα για πρόβατα
Active substance:
- Chlamydia abortus, Inactivated
Target species:
-
Sheep
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Chlamydia abortus, Inactivated5.00/log 10 50% embryo lethal dose2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal, milk0day
-
-
-
Subcutaneous use
-
Sheep
-
Meat and offal, milk0day
-
-
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 130059/30-11-2022/K-0123801
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.
Greek (PDF)
Published on: 26/08/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Greek (PDF)
Published on: 26/08/2024