Veterinary Medicines

ACTIONIS 50 mg/ml, suspension for injection for pigs and cattle

Authorised
  • Ceftiofur hydrochloride
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Product identification

Medicine name:
ACTIONIS 50 mg/ml, suspension for injection for pigs and cattle
Actionis 50 mg/ml, sospensione iniettabile per bovini e suini
Active substance:
  • Ceftiofur hydrochloride
Target species:
  • Pig
  • Cattle
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Ceftiofur hydrochloride
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        6
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        6
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01DD90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
Package description:
  • box containing 1 PET vial of 250 ml
  • box containing 1 PET vial of 100 ml
  • box containing 1 glass vial of 250 ml
  • box containing 1 glass vial of 100 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Laboratorios Syva S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Syva S.A.U.
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 104289
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0157/001
Concerned member states:
  • Germany
  • Hungary
  • Italy
  • Poland
  • Portugal
  • United Kingdom (Northern Ireland)

Documents

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Italian (PDF)
Published on: 20/12/2023
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