Drontal Oral Suspension for Puppies 15/5 mg/ml
Drontal Oral Suspension for Puppies 15/5 mg/ml
Authorised
- Febantel
- Pyrantel embonate
Product identification
Medicine name:
Drontal Oral Suspension for Puppies 15/5 mg/ml
Welpan vet. 15 mg/ml + 5 mg/ml mikstur, suspensjon
Active substance:
- Febantel
- Pyrantel embonate
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Febantel15.00/milligram(s)1.00millilitre(s)
-
Pyrantel embonate14.40/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Norway
Package description:
- Material of the primary container:White high density polyethylene bottle.White polypropylene screw closure.Colourless low density polyethylene adapter insert.Container volume:100ml.Devices supplied (if relevant):5ml transparent polypropylene syringe with rubber plunger.
- Material of the primary container:White high density polyethylene bottle.White polypropylene screw closure.Colourless low density polyethylene adapter insert.Container volume:50ml.Devices supplied (if relevant):5ml transparent polypropylene syringe with rubber plunger.
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+Veterinaer Produkte GmbH
- Vetoquinol Biowet Sp. z o.o.
Responsible authority:
- Norwegian Medical Products Agency
Authorisation number:
- 07-5484
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0473/001
Concerned member states:
-
Austria
-
Estonia
-
Finland
-
France
-
Germany
-
Iceland
-
Latvia
-
Lithuania
-
Norway
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Norwegian (PDF)
Published on: 26/01/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Norwegian (PDF)
Published on: 10/12/2024
Combined File of all Documents
English (PDF)
Download Published on: 16/11/2025
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