Veterinary Medicines

Tauramox 5 mg/ml Pour-On Solution for Cattle

Authorised
  • Moxidectin
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Product identification

Medicine name:
Tauramox 5 mg/ml Pour-On Solution for Cattle
Tauramox 5 mg/ml Pour-On Solution for Cattle
Active substance:
  • Moxidectin
Target species:
  • Cattle
Route of administration:
  • Pour-on use

Product details

Active substance and strength:
  • Moxidectin
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Pour-on solution
Withdrawal period by route of administration:
  • Pour-on use
    • Cattle
      • Meat and offal
        14
        day
      • Milk
        144
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
Package description:
  • The product will be supplied in:1L fluorinated high density polyethylene single neck dispensers with high density polyethylene/polypropylene caps and green fluorinated high density polyethylene ball plugs.
  • The product will be supplied in:250mL fluorinated high density polyethylene single neck dispensers with high density polyethylene/polypropylene caps and green fluorinated high density polyethylene ball plugs.
  • The product will be supplied in:1L white fluorinated flat high density polyethylene back-packs with white polypropylene easy peel caps.
  • The product will be supplied in:2.5L white fluorinated flat high density polyethylene back-packs with white polypropylene easy peel caps.
  • The product will be supplied in:5L white fluorinated flat high density polyethylene back-packs with white polypropylene easy peel caps.
  • The product will be supplied in:10L white high density polyethylene fluorinated jerry can with white high density polyethylene cap

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:
  • Norbrook Laboratories Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Manufacturing Ltd
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 02000/4406
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0600/001
Concerned member states:
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 9/01/2024
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