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Suivac APP injekčná emulzia

Authorised
  • Actinobacillus pleuropneumoniae, Inactivated
  • Actinobacillus pleuropneumoniae, Inactivated
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Product identification

Medicine name:
Suivac APP injekčná emulzia
Active substance:
  • Actinobacillus pleuropneumoniae, Inactivated
  • Actinobacillus pleuropneumoniae, Inactivated
Target species:
  • Pig
  • Pig
Route of administration:
  • Intradermal use
  • Intramuscular use

Product details

Active substance and strength:
  • Actinobacillus pleuropneumoniae, Inactivated
    1.00
    billion colony forming units
    /
    0.20
    millilitre(s)
  • Actinobacillus pleuropneumoniae, Inactivated
    1.00
    billion colony forming units
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intradermal use
    • Pig
      • All relevant tissues
        0
        day
  • Intramuscular use
    • Pig
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
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:
  • Dyntec spol. s r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Dyntec spol. s r.o.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/021/02-S
Date of authorisation status change:

Documents

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Published on: 16/12/2021
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