Kolierysin Neo injekčná emulzia
Kolierysin Neo injekčná emulzia
Authorised
- Escherichia coli (inactivated)
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated
- Erysipelothrix rhusiopathiae, serotype 1, strain 203, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated
Product identification
Medicine name:
Kolierysin Neo injekčná emulzia
Active substance:
- Escherichia coli (inactivated)
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated
- Erysipelothrix rhusiopathiae, serotype 1, strain 203, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Escherichia coli (inactivated)54.00billion colony forming units2.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated200.00billion colony forming units2.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated200.00billion colony forming units2.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 1, strain 203, Inactivated200.00billion colony forming units2.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated200.00billion colony forming units2.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
All relevant tissues0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
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:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/018/02-S
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
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Slovak (PDF)
Published on: 7/11/2023
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