OVAX CLAMIDIA
OVAX CLAMIDIA
Authorised
- Chlamydia abortus, Inactivated
- Chlamydia abortus, Inactivated
Product identification
Medicine name:
OVAX CLAMIDIA
Active substance:
- Chlamydia abortus, Inactivated
- 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)
-
Chlamydia abortus, Inactivated5.00/log 10 50% embryo lethal dose2.00Dose
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal0day
-
Milk0hour
-
-
-
Subcutaneous use
-
Sheep
-
Meat and offal0day
-
Milk0hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI10BV
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Ministry Of Health
Authorisation number:
- 100225
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 14/09/2022