Veterinary Medicines

Taurador 5 mg/ml Pour-on Solution for Cattle

Authorised
  • Doramectin
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Product identification

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

Product details

Active substance and strength:
  • Doramectin
    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
        35
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • The veterinary product will be supplied in:20L white high density polyethylene Jerry cans with high density polyethylene caps.
  • The veterinary product will be supplied in:10L white high density polyethylene Jerry cans with high density polyethylene caps.
  • The veterinary product will be supplied in:5L white flat bottomed heavy duty high density polyethylene back-packs with 38mm white polypropylene easy peel caps.
  • The veterinary product will be supplied in:2.5L white flat bottomed heavy duty high density polyethylene back-packs with 38mm white polypropylene easy peel caps.
  • The veterinary product will be supplied in:1L white flat bottomed heavy duty high density polyethylene back-packs with 38mm white polypropylene easy peel caps.
  • The veterinary product will be supplied in:1L standard high density polyethylene bottles with 28mm polypropylene/high density polyethylene caps.
  • The veterinary product will be supplied in:250mL standard high density polyethylene bottles with 28mm polypropylene/high density polyethylene caps.

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 (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Laboratories (Ireland) Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA22664/111/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0617/001
Concerned member states:
  • Austria
  • Belgium
  • France
  • Luxembourg
  • Netherlands
  • Portugal
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 18/01/2026
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Combined File of all Documents

English (PDF)
Published on: 18/01/2026
Download