Veterinary Medicines Information website

Levapharm Injection 75 mg/ml

Authorised
  • Levamisole hydrochloride
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Product identification

Medicine name:
Levapharm Injection 75 mg/ml
Active substance:
  • Levamisole hydrochloride
Target species:
  • Cattle
  • Sheep
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Levamisole hydrochloride
    88.39
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        14
        day
    • Sheep
      • Meat and offal
        14
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AE01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • The veterinary medicinal product is supplied in glass vials in a cardboard box, sealed with bromobutyl bung and aluminium seals. Package size: 1 x 100 ml vial in a cardboard box
  • The veterinary medicinal product is supplied in glass vials in a cardboard box, sealed with bromobutyl bung and aluminium seals. Package size: 1 x 250 ml vial in a cardboard box
  • The veterinary medicinal product is supplied in glass vials in a cardboard box, sealed with bromobutyl bung and aluminium seals. Package size: 1 x 500 ml vial in a cardboard box
  • The veterinary medicinal product is supplied in glass vials in a cardboard box, sealed with bromobutyl bung and aluminium seals. Package size: 6 x 500 ml vials with 1 protective container in a cardboard box.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Informed consent application (Article 13c of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Chem-Pharm (Ballyvaughan) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Laboratories Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10823/010/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 7/06/2026
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