Veterinary Medicines

Gletvax 6 suspensão injetável para suínos

Authorised
  • Clostridium perfringens, epsilon toxoid
  • Clostridium perfringens, type B and C, beta toxoid
  • Escherichia coli, fimbrial adhesin F6
  • Escherichia coli, fimbrial adhesin F5
  • Escherichia coli, fimbrial adhesin F4ac
  • Escherichia coli, fimbrial adhesin F4ab
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Product identification

Medicine name:
Gletvax 6 suspensão injetável para suínos
Active substance:
  • Clostridium perfringens, epsilon toxoid
  • Clostridium perfringens, type B and C, beta toxoid
  • Escherichia coli, fimbrial adhesin F6
  • Escherichia coli, fimbrial adhesin F5
  • Escherichia coli, fimbrial adhesin F4ac
  • Escherichia coli, fimbrial adhesin F4ab
Target species:
  • Pig (pregnant sow)
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Clostridium perfringens, epsilon toxoid
    300.00
    unit(s)
    /
    1.00
    Other
  • Clostridium perfringens, type B and C, beta toxoid
    350.00
    unit(s)
    /
    1.00
    Other
  • Escherichia coli, fimbrial adhesin F6
  • Escherichia coli, fimbrial adhesin F5
  • Escherichia coli, fimbrial adhesin F4ac
  • Escherichia coli, fimbrial adhesin F4ab
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig (pregnant sow)
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Pig (pregnant sow)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB08
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Portugal
Package description:

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:
  • Zoetis Portugal Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 506/93 DGV
Date of authorisation status change:

Documents

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Published on: 20/06/2023
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