Veterinary Medicines

Drontal Tasty Bone Multi-worm 150/144/50 mg tablets

Authorised
  • Febantel
  • Praziquantel
  • Pyrantel embonate
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Product identification

Medicine name:
Drontal Tasty Bone Multi-worm 150/144/50 mg tablets
Drontal Plus 150/144/50 mg ízesített tabletta A.U.V.
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
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Hungary
Available in:
  • Hungary
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:
  • Europeenne De Pharmacotechnie Europhartech
  • KVP Pharma+Veterinaer Produkte GmbH
Responsible authority:
  • Directorate Of Veterinary Medicinal Products
Authorisation number:
  • 3602/X/14 NÉBIH ÁTI
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0337/001
Concerned member states:
  • Bulgaria
  • Croatia
  • Cyprus
  • Denmark
  • Estonia
  • Greece
  • Hungary
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovenia
  • Spain

Documents

Summary of Product Characteristics

English (PDF)
Published on: 25/09/2024
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