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Oramec Drench vet. 0,8 mg/ml Mixtúra, lausn Handa sauðfé og geitum.

Authorised
  • Ivermectin
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Product identification

Medicine name:
Oramec Drench vet. 0,8 mg/ml Mixtúra, lausn Handa sauðfé og geitum.
Active substance:
  • Ivermectin
Target species:
  • Sheep
  • Goat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Ivermectin
    0.80
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral solution
Withdrawal period by route of administration:
  • Oral use
    • Sheep
      • Meat and offal
        6
        day
    • Goat
      • Meat and offal
        8
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Iceland
Available in:
  • Iceland
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone)
Marketing authorisation holder:
  • Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
  • Merck Sharp & Dohme B.V.
Responsible authority:
  • Icelandic Medicines Agency
Authorisation number:
  • 910066
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Icelandic (PDF)
Published on: 18/01/2022
Updated on: 5/11/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Icelandic (PDF)
Published on: 18/01/2022
Updated on: 5/11/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Icelandic (PDF)
Published on: 5/11/2025
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