Veterinary Medicines

Interflox-100, 100 mg/ml solution for injection for cattle, sheep, goats and pigs

Authorised
  • Enrofloxacin
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Product identification

Medicine name:
Interflox-100, 100 mg/ml solution for injection for cattle, sheep, goats and pigs
Interflox-100, 100 mg/ml injekčný roztok pre hovädzí dobytok, ovce, kozy a ošípané
Active substance:
  • Enrofloxacin
Target species:
  • Cattle
  • Sheep
  • Goat
  • Pig
Route of administration:
  • Intravenous use
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Enrofloxacin
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        5
        day
      • Milk
        3
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        12
        day
      • Milk
        4
        day
    • Sheep
      • Meat and offal
        4
        day
      • Milk
        3
        day
    • Goat
      • Meat and offal
        6
        day
      • Milk
        4
        day
  • Intramuscular use
    • Pig
      • Meat and offal
        13
        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
Package description:
  • 100 ml amber glass bottles (type I) closed with brombutyl rubber stopper and aluminium cap in cardboard box.

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:
  • Interchemie Werken De Adelaar Eesti AS
Marketing authorisation date:
Manufacturing sites for batch release:
  • Interchemie Werken De Adelaar Eesti AS
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/017/MR/19-S
Date of authorisation status change:
Reference member state:
  • Estonia
Procedure number:
  • EE/V/0103/001
Concerned member states:
  • Austria
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • France
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Malta
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
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