Veterinary Medicines

Noromectin 10 mg/ml Solution for Injection for sheep.

Authorised
  • Ivermectin
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Product identification

Medicine name:
Noromectin 10 mg/ml Solution for Injection for sheep.
Noromectin 10 mg/ml Solution for Injection for sheep.
Active substance:
  • Ivermectin
Target species:
  • Sheep
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Ivermectin
    10.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Sheep
      • Meat and offal
        42
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • The product will be supplied as a colourless to pale yellow solution in 50 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
  • The product will be supplied as a colourless to pale yellow solution in 100 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
  • The product will be supplied as a colourless to pale yellow solution in 250 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
  • The product will be supplied as a colourless to pale yellow solution in 500 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
  • The product will be supplied as a colourless to pale yellow solution in 1 L volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Manufacturing Limited
  • Norbrook Laboratories Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA22664/059/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0168/001
Concerned member states:
  • Italy
  • Portugal
  • Spain

Documents

Summary of Product Characteristics

English (PDF)
Published on: 19/10/2025
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Combined File of all Documents

English (PDF)
Published on: 19/10/2025
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