Veterinary Medicines

Drontal Tasty Bone Multi-worm XL 525/504/175 mg tablets

Authorised
  • Febantel
  • Praziquantel
  • Pyrantel embonate
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Product identification

Medicine name:
Drontal Tasty Bone Multi-worm XL 525/504/175 mg tablets
Drontal Dog Flavour XL 525 mg + 504 mg + 175 mg Tabletka
Active substance:
  • Febantel
  • Praziquantel
  • Pyrantel embonate
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Febantel
    525.00
    milligram(s)
    /
    1.00
    Tablet
  • Praziquantel
    175.00
    milligram(s)
    /
    1.00
    Tablet
  • Pyrantel embonate
    504.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AA51
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Available in:
  • Poland
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 8 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 48 tablets.

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:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Europeenne De Pharmacotechnie Europhartech
  • KVP Pharma+Veterinaer Produkte GmbH
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 2754
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0337/002
Concerned member states:
  • Bulgaria
  • Croatia
  • Cyprus
  • Estonia
  • Greece
  • Hungary
  • Latvia
  • Lithuania
  • Poland
  • Portugal
  • Romania
  • Slovenia
  • Spain

Documents

Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/09/2023
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Summary of Product Characteristics

English (PDF)
Published on: 26/08/2024
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Polish (PDF)
Published on: 4/09/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 14/11/2024
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