Veterinary Medicines

Drontal Tasty Bone Wormer XL 525/504/175 mg tablets

Authorised
  • Febantel
  • Pyrantel embonate
  • Praziquantel
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Product identification

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

Product details

Active substance and strength:
  • Febantel
    525.00
    milligram(s)
    /
    1.00
    Tablet
  • Pyrantel embonate
    504.00
    milligram(s)
    /
    1.00
    Tablet
  • Praziquantel
    175.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Withdrawal period by route of administration:
  • Oral use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AA51
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • Container material: Blisters formed from PA/Alu/PE foil and sealed with Alu/PE foil.Container size: Cartons containing 48 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 8 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 2 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:
  • KVP Pharma+Veterinär Produkte GmbH
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10521/015/002
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0338/002
Concerned member states:
  • Belgium
  • Czechia
  • Luxembourg
  • Slovakia

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
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