Veterinary Medicines

Solantel 50mg/ml Oral Suspension for Sheep

Authorised
  • Closantel sodium dihydrate
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Product identification

Medicine name:
Solantel 50 mg/ml Oral Suspension for Sheep
Solantel 50mg/ml Oral Suspension for Sheep
Active substance:
  • Closantel sodium dihydrate
Target species:
  • Sheep
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Closantel sodium dihydrate
    54.38
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Sheep
      • Meat and offal
        56
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AG09
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
Available in:
  • United Kingdom (Northern Ireland)
Package description:
  • White high density polyethylene multidose container backpacks with high density polyethylene screw cap with induction-sealliners. Pack sizes:Box with 1 multidose container of 1 litre
  • White high density polyethylene multidose container backpacks with high density polyethylene screw cap with induction-sealliners. Pack sizes:Box with 1 multidose container of 2.5 litres
  • White high density polyethylene multidose container backpacks with high density polyethylene screw cap with induction-sealliners. Pack sizes:Box with 1 multidose container of 5 litres

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 Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Manufacturing Limited
  • Norbrook Laboratories Limited
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 02000/4402
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0552/001
Concerned member states:
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 12/10/2025
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Combined File of all Documents

English (PDF)
Published on: 12/10/2025
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