FIXR Coli
FIXR Coli
Authorised
- Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
- Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
- Escherichia coli, serotype O147:K88 (fimbrial adhesin F4ab), Inactivated
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Escherichia coli, serotype O149:K88 (fimbrial adhesin F4ac), Inactivated
Product identification
Medicine name:
FIXR Coli
Active substance:
- Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated
- Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated
- Escherichia coli, serotype O147:K88 (fimbrial adhesin F4ab), Inactivated
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Escherichia coli, serotype O149:K88 (fimbrial adhesin F4ac), Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Escherichia coli, serotype O101:K99 (fimbrial adhesins F5 and F41), Inactivated1.00/relative potency2.00millilitre(s)
-
Escherichia coli, serotype K85:987P (fimbrial adhesin F6), Inactivated1.00/relative potency2.00millilitre(s)
-
Escherichia coli, serotype O147:K88 (fimbrial adhesin F4ab), Inactivated1.00/relative potency2.00millilitre(s)
-
Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated1.00/relative potency2.00millilitre(s)
-
Escherichia coli, serotype O149:K88 (fimbrial adhesin F4ac), Inactivated1.00/relative potency2.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- 1 × 10 ml, glass vial airtight sealed with rubber pierceable stoppers and fitted with aluminium caps, inserted into cardboard boxes.
- 1 × 100 ml glass vial airtight sealed with rubber pierceable stoppers and fitted with aluminium caps, inserted into cardboard boxes.
- 1 × 100 ml plastic vial of 120 ml airtight sealed with rubber pierceable stoppers and fitted with aluminium caps, inserted into cardboard boxes.
- 1 × 20 ml glass vial airtight sealed with rubber pierceable stoppers and fitted with aluminium caps, inserted into cardboard boxes.
- 1 × 50 ml glass vial airtight sealed with rubber pierceable stoppers and fitted with aluminium caps, inserted into cardboard boxes.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Similar biological application (Article 13(4) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Kernfarm B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0332/001
Concerned member states:
-
Belgium
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Combined File of all Documents
English (PDF)
Download Published on: 24/04/2025
Labelling
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