Drontal, film coated tablet
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 embonate230.00milligram(s)1.00Tablet
-
Praziquantel20.00milligram(s)1.00Tablet
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:
-
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
Legal basis of product authorisation:
-
Full application (Article 12(3) 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:
- 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
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 16/02/2022
French (PDF)
Published on: 4/04/2022
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