OVICON
OVICON
Authorised
- Dichelobacter nodosus, Inactivated
- Fusobacterium necrophorum, Inactivated
- STAPHYLOCOCCUS AUREUS
- Trueperella pyogenes, Inactivated
- Clostridium perfringens, serotype A, Inactivated
Product identification
Medicine name:
ОВИКОН
OVICON
Active substance:
- Dichelobacter nodosus, Inactivated
- Fusobacterium necrophorum, Inactivated
- STAPHYLOCOCCUS AUREUS
- Trueperella pyogenes, Inactivated
- Clostridium perfringens, serotype A, Inactivated
Target species:
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Dichelobacter nodosus, Inactivated4.00billion colony forming units1.00millilitre(s)
-
Fusobacterium necrophorum, Inactivated4.00billion colony forming units1.00millilitre(s)
-
STAPHYLOCOCCUS AUREUS2.00billion colony forming units1.00millilitre(s)
-
Trueperella pyogenes, Inactivated2.00billion colony forming units1.00millilitre(s)
-
Clostridium perfringens, serotype A, Inactivated1.00billion colony forming units1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Sheep
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI04AV
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Mintech Co EOOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Mintech Co EOOD
Responsible authority:
- BFSA
Authorisation number:
- 0022-2063
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.
Bulgarian (PDF)
Published on: 6/06/2022
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 6/06/2022
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