KOLISIN Neo, emulsie injectabilă
KOLISIN Neo, emulsie injectabilă
Not authorised
- Escherichia coli, fimbrial adhesin F6
- Escherichia coli, fimbrial adhesin F5
- Escherichia coli, fimbrial adhesin F4 (F4ab, F4ac, F4ad)
- Escherichia coli, fimbrial adhesin F41
Product identification
Medicine name:
KOLISIN Neo, emulsie injectabilă
Active substance:
- Escherichia coli, fimbrial adhesin F6
- Escherichia coli, fimbrial adhesin F5
- Escherichia coli, fimbrial adhesin F4 (F4ab, F4ac, F4ad)
- Escherichia coli, fimbrial adhesin F41
Target species:
-
Pig (pregnant sow)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Escherichia coli, fimbrial adhesin F61.00/relative potency2.00millilitre(s)
-
Escherichia coli, fimbrial adhesin F51.00/relative potency2.00millilitre(s)
-
Escherichia coli, fimbrial adhesin F4 (F4ab, F4ac, F4ad)1.00/relative potency2.00millilitre(s)
-
Escherichia coli, fimbrial adhesin F411.00/relative potency2.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig (pregnant sow)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB02
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Surrendered
Authorised in:
-
Romania
Package description:
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
- Available only in Romanian
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 Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 140072
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.
Romanian (PDF)
Published on: 8/12/2021