Veterinary Medicines Information website

Curafluke 10% w/v Oral Drench

Authorised
  • Fenbendazole
  • Rafoxanide
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Product identification

Medicine name:
Curafluke 10% w/v Oral Drench
Active substance:
  • Fenbendazole
  • Rafoxanide
Target species:
  • Cattle
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Fenbendazole
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Rafoxanide
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        60
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AC30
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • 5 L (backpack) HDPE white rigid containers closed with a polypropylene screw cap with an induction heat seal liner. The product may be marketed with or without an outer carton.
  • 2.5 L (back pack) HDPE white rigid containers closed with a polypropylene screw cap with an induction heat seal liner. The product may be marketed with or without an outer carton.
  • 1 L (back pack) HDPE white rigid containers closed with a polypropylene screw cap with an induction heat seal liner. The product may be marketed with or without an outer carton.
  • 5 L (jerrican) HDPE white rigid containers closed with a polypropylene screw cap with an induction heat seal liner. The product may be marketed with or without an outer carton.
  • 2.5 L (jerrican) HDPE white rigid containers closed with a polypropylene screw cap with an induction heat seal liner. The product may be marketed with or without an outer carton.
  • 1 L (jerrican) HDPE white rigid containers closed with a polypropylene screw cap with an induction heat seal liner. The product may be marketed with or without an outer carton.

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:
  • Univet Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Univet Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10990/032/002
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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