Veterinary Medicines

Dehinel 230 mg/20 mg film-coated tablets for cats

Authorised
  • Praziquantel
  • Pyrantel embonate
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Product identification

Medicine name:
Dehinel 230 mg/20 mg film-coated tablets for cats
ANTHELMIN 230 mg/20 mg επικαλυμμένα με λεπτό υμένιο δισκία για γάτες
Active substance:
  • Praziquantel
  • Pyrantel embonate
Target species:
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Praziquantel
    20.00
    milligram(s)
    /
    1.00
    Tablet
  • Pyrantel embonate
    230.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Film-coated tablet
Withdrawal period by route of administration:
  • Oral use
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AA51
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Greece
Package description:
  • (ID3) 10 Film-coated tablet: unspecified outer container with 1 Blister (Orientated PolyAmide; Aluminium; PolyVinyl Chloride) with 10 Film-coated tablet, closed with Foil (Aluminium)
  • (ID2) 4 Film-coated tablet: unspecified outer container with 2 Blister (Orientated PolyAmide; Aluminium; PolyVinyl Chloride) each with 2 Film-coated tablet, closed with Foil (Aluminium)
  • (ID1) 2 Film-coated tablet: unspecified outer container with 1 Blister (Orientated PolyAmide; Aluminium; PolyVinyl Chloride) with 2 Film-coated tablet, closed with Foil (Aluminium)

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:
  • KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
  • KRKA tovarna zdravil d.d. Novo mesto
  • TAD Pharma GmbH
  • Krka-Farma d.o.o.
  • Krka-Farma d.o.o.
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 71598/04-07-2023/K-0227401
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0160/002
Concerned member states:
  • Cyprus
  • France
  • Greece
  • Italy
  • Poland

Documents

Combined File of all Documents

English (PDF)
Published on: 14/06/2024
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Greek (PDF)
Published on: 4/08/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Greek (PDF)
Published on: 4/08/2023
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