Veterinary Medicines

Zanil Fluke Drench

Authorised
  • Oxyclozanide
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Product identification

Medicine name:
Zanil Fluke Drench
Active substance:
  • Oxyclozanide
Target species:
  • Cattle
  • Sheep
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Oxyclozanide
    3.40
    gram(s)
    /
    100.00
    millilitre(s)
Pharmaceutical form:
  • Oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Milk
        72
        hour
    • Sheep
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52A
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • High density polyethylene back-packs of 5 litre nominal volume. Closure: Polypropylene or urea formaldehyde screw cap with wads of PVDC-faced paper on a pulpboard liner.
  • High density polyethylene back-packs of 2.5 litre nominal volume. Closure: Polypropylene or urea formaldehyde screw cap with wads of PVDC-faced paper on a pulpboard liner.
  • High density polyethylene back-packs of 1 litre nominal volume. Closure: Polypropylene or urea formaldehyde screw cap with wads of PVDC-faced paper on a pulpboard liner.
  • High density polyethylene bottles of 10 litre nominal volume. Closure: Polypropylene or urea formaldehyde screw cap with wads of PVDC-faced paper on a pulpboard liner.
  • High density polyethylene bottles of 5 litre nominal volume. Closure: Polypropylene or urea formaldehyde screw cap with wads of PVDC-faced paper on a pulpboard liner.
  • High density polyethylene bottles of 2.5 litre nominal volume. Closure: Polypropylene or urea formaldehyde screw cap with wads of PVDC-faced paper on a pulpboard liner.
  • High density polyethylene bottles of 1 litre nominal volume. Closure: Polypropylene or urea formaldehyde screw cap with wads of PVDC-faced paper on a pulpboard liner.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Trirx Segre
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/262/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

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