Veterinary Medicines Information website

Noromectin Multi Injection Solution for Injection

Authorised
  • Ivermectin
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Product identification

Medicine name:
Noromectin Multi Injection Solution for Injection
Active substance:
  • Ivermectin
Target species:
  • Cattle
  • Sheep
  • Pig
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
    • Cattle
      • Meat and offal
        49
        day
    • Sheep
      • Meat and offal
        42
        day
    • Pig
      • Meat and offal
        28
        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
Available in:
  • Ireland
Package description:
  • Noromectin Multi Injection will be supplied in a 1.5 litre (1 x 1 litre and 1 x 500ml) combination pack.
  • Noromectin Multi Injection will be supplied in 50 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
  • Noromectin Multi Injection will be supplied in 100 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
  • Noromectin Multi Injection will be supplied in 250 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
  • Noromectin Multi Injection will be supplied in 500 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
  • Noromectin Multi Injection will be supplied in 1 litre volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Informed consent (abridged application) - Council Directive 81/851/EEC
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:
  • VPA22664/068/001
Date of authorisation status change:

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
Download