Skip to main content
Veterinary Medicines

Drontal Tasty Bone Wormer 150/144/50 mg tablets

Authorised
  • Febantel
  • Praziquantel
  • Pyrantel embonate

Product identification

Medicine name:
Drontal Tasty Bone Wormer 150/144/50 mg tablets
Active substance:
  • Febantel
  • Praziquantel
  • Pyrantel embonate
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Febantel
    150.00
    milligram(s)
    /
    1.00
    Tablet
  • Praziquantel
    50.00
    milligram(s)
    /
    1.00
    Tablet
  • Pyrantel embonate
    144.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AC55
Authorisation status:
  • Valid
Authorised in:
  • Luxembourg
Available in:
  • Luxembourg
Package description:
  • Container material: Blisters formed from PA/Alu/PE foil and sealed with Alu/PE foil.Container size: Cartons containing 2 tablets
  • Container material: Blisters formed from PA/Alu/PE foil and sealed with Alu/PE foil.Container size: Cartons containing 4 tablets
  • Container material: Blisters formed from PA/Alu/PE foil and sealed with Alu/PE foil.Container size: Cartons containing 6 tablets
  • Container material: Blisters formed from PA/Alu/PE foil and sealed with Alu/PE foil.Container size: Cartons containing 24 tablets
  • Container material: Blisters formed from PA/Alu/PE foil and sealed with Alu/PE foil.Container size: Cartons containing 102 tablets
  • Container material: Blisters formed from PA/Alu/PE foil and sealed with Alu/PE foil.Container size: Cartons containing 312 tablets

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Europeenne De Pharmacotechnie Europhartech
  • KVP Pharma+Veterinaer Produkte GmbH
Responsible authority:
  • Ministry Of Health And Social Security
Authorisation number:
  • V 808/14/09/2160
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0338/001
Concerned member states:
  • Belgium
  • Czechia
  • Luxembourg
  • Slovakia

Documents

Summary of Product Characteristics

English (PDF)
Published on: 26/08/2024
Download
French (PDF)
Published on: 7/04/2025

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 7/04/2025
German (PDF)
Published on: 7/04/2025

Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 7/04/2025
German (PDF)
Published on: 7/04/2025