Veterinary Medicines

Drontal Dog Tasty Bone 150/144/50 mg tablets

Authorised
  • Praziquantel
  • Pyrantel embonate
  • Febantel
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Product identification

Medicine name:
Drontal Dog Tasty Bone 150/144/50 mg tablets
Drontal Plus Tasty 150/144/50 mg Tabletten für Hunde
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
Withdrawal period by route of administration:
  • Oral use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AC55
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
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
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+Veterinaer Produkte GmbH
  • Europeenne De Pharmacotechnie Europhartech
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 402045.00.00
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0335/001
Concerned member states:
  • Austria
  • Denmark
  • Finland
  • France
  • Germany
  • Iceland
  • Italy
  • Netherlands
  • Norway
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

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German (PDF)
Published on: 1/10/2024
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