Veterinary Medicines

TOXICOL VET, injekcinė suspensija

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

Medicine name:
TOXICOL VET, injekcinė suspensija
Active substance:
  • Escherichia coli, fimbrial adhesin F4ab
  • Escherichia coli, fimbrial adhesin F4ac
  • Escherichia coli, fimbrial adhesin F6
  • Escherichia coli, fimbrial adhesin F5
  • Clostridium perfringens, type B and C, beta toxoid
  • Clostridium perfringens, type D, epsilon toxoid
Target species:
  • Pig
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

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

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • State Food And Veterinary Service
Authorisation number:
  • LT/2/04/1618/001-002
Date of authorisation status change:

Documents

RV1618.PDF

Lithuanian (PDF)
Published on: 27/07/2022
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