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Enroxil 50 mg/ml injekčný roztok pre hovädzí dobytok (teľatá), ovce, kozy, ošípané a psy

Authorised
  • Enrofloxacin
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Product identification

Medicine name:
Enroxil 50 mg/ml injekčný roztok pre hovädzí dobytok (teľatá), ovce, kozy, ošípané a psy
Active substance:
  • Enrofloxacin
Target species:
  • Cattle (calf)
  • Pig
  • Sheep
  • Goat
  • Dog
Route of administration:
  • Intravenous use
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Enrofloxacin
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle (calf)
      • Meat and offal
        5
        day
  • Intramuscular use
    • Pig
      • Meat and offal
        13
        day
  • Subcutaneous use
    • Cattle (calf)
      • Meat and offal
        12
        day
    • Sheep
      • Meat and offal
        4
        day
      • Milk
        3
        day
    • Goat
      • Meat and offal
        6
        day
      • Milk
        4
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Available in:
  • Slovakia
Package description:

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:
  • KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
  • KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/0012/95-S
Date of authorisation status change:

Documents

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Slovak (PDF)
Published on: 6/10/2023
Updated on: 8/10/2023
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