Veterinary Medicines

Drontal Plus Tablets

Authorised
  • Praziquantel
  • Pyrantel embonate
  • Febantel
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Product identification

Medicine name:
Drontal Plus Tablets
Active substance:
  • Praziquantel
  • Pyrantel embonate
  • Febantel
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Praziquantel
    50.00
    milligram(s)
    /
    1.00
    Tablet
  • Pyrantel embonate
    144.00
    milligram(s)
    /
    1.00
    Tablet
  • Febantel
    150.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AA51
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • Container: Aluminium foil blister or polyethylene-coated aluminium blister.Container colour: Silver or white colouredContainer sizes: Cartons containing 100 tablets.Contents: Pale yellow tablets
  • Container: Aluminium foil blister or polyethylene-coated aluminium blister.Container colour: Silver or white colouredContainer sizes: Cartons containing 20 tablets.Contents: Pale yellow tablets
  • Container: Aluminium foil blister or polyethylene-coated aluminium blister.Container colour: Silver or white colouredContainer sizes: Cartons containing 6 tablets.Contents: Pale yellow tablets
  • Container: Aluminium foil blister or polyethylene-coated aluminium blister.Container colour: Silver or white colouredContainer sizes: Cartons containing 4 tablets.Contents: Pale yellow tablets
  • Container: Aluminium foil blister or polyethylene-coated aluminium blister.Container colour: Silver or white colouredContainer sizes: Cartons containing 2 tablets.Contents: Pale yellow tablets

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • KVP Pharma+Veterinaer Produkte GmbH
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10521/006/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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