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Veterinary Medicines

Drontal, film coated tablet

Authorised
  • Pyrantel embonate
  • Praziquantel

Product identification

Medicine name:
Drontal, film coated tablet
DRONTAL CHAT
Active substance:
  • Pyrantel embonate
  • Praziquantel
Target species:
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Pyrantel embonate
    230.00
    milligram(s)
    /
    1.00
    Tablet
  • Praziquantel
    20.00
    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
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:
  • (ID5) 4 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 4 Film-coated tablet
  • (ID1) 2 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 2 Film-coated tablet
  • (ID8) 96 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 96 Film-coated tablet
  • (ID2) 20 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 20 Film-coated tablet
  • (ID4) 100 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 100 Film-coated tablet
  • (ID7) 24 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 24 Film-coated tablet
  • (ID9) 144 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 144 Film-coated tablet
  • (ID3) 6 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 6 Film-coated tablet
  • (ID6) 8 Film-coated tablet: unspecified outer container with 1 Cello pack (Aluminium; PolyEthylene) with 8 Film-coated tablet

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • KVP Pharma+Veterinär Produkte GmbH
Responsible authority:
  • National Veterinary Medicines Agency
Authorisation number:
  • FR/V/0272772 1/1996
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0101/001
Concerned member states:
  • France
  • Spain

Documents

Summary of Product Characteristics

English (PDF)
Published on: 16/02/2022
Download
French (PDF)
Published on: 4/04/2022
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