GLETVAX 6 συνδυασμένο εμβόλιο χοίρου για την πρόληψη της κολοβακτηριδιάσεων και της νεκρωτικής εντερίτιδας των χοίριδίων
GLETVAX 6 συνδυασμένο εμβόλιο χοίρου για την πρόληψη της κολοβακτηριδιάσεων και της νεκρωτικής εντερίτιδας των χοίριδίων
Authorised
- Escherichia coli, serotype O149:K88 (fimbrial adhesin F4), Inactivated
- Escherichia coli, strain O8:K87, K88, fimbrial adhesin F4, Inactivated
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Escherichia coli, serotype O9 (fimbrial adehsin F6), Inactivated
- Clostridium perfringens, type B, C and D, beta toxoid
Product identification
Medicine name:
GLETVAX 6 συνδυασμένο εμβόλιο χοίρου για την πρόληψη της κολοβακτηριδιάσεων και της νεκρωτικής εντερίτιδας των χοίριδίων
Active substance:
- Escherichia coli, serotype O149:K88 (fimbrial adhesin F4), Inactivated
- Escherichia coli, strain O8:K87, K88, fimbrial adhesin F4, Inactivated
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Escherichia coli, serotype O9 (fimbrial adehsin F6), Inactivated
- Clostridium perfringens, type B, C and D, beta toxoid
Target species:
-
Pig (piglet)
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Escherichia coli, serotype O149:K88 (fimbrial adhesin F4), Inactivated15.50log2 antibody unit(s)5.00millilitre(s)
-
Escherichia coli, strain O8:K87, K88, fimbrial adhesin F4, Inactivated14.60log2 antibody unit(s)5.00millilitre(s)
-
Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated12.20log2 antibody unit(s)5.00millilitre(s)
-
Escherichia coli, serotype O9 (fimbrial adehsin F6), Inactivated13.10log2 antibody unit(s)5.00millilitre(s)
-
Clostridium perfringens, type B, C and D, beta toxoid300.00international unit(s)5.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Pig (piglet)
-
Intramuscular use
- Pig (piglet)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB08
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Package description:
- Available only in Greek
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:
- Zoetis Hellas S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Ministry Of Agriculture Rural Development And Environment
Authorisation number:
- 19170
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
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Greek (PDF)
Published on: 11/07/2022
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