Drontal Tasty Bone Wormer 150/144/50 mg tablets
Drontal Tasty Bone Wormer 150/144/50 mg tablets
Authorised
- Febantel
- Praziquantel
- Pyrantel embonate
Product identification
Medicine name:
Drontal Tasty Bone Wormer 150/144/50 mg tablets
Active substance:
- Febantel
- Praziquantel
- Pyrantel embonate
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Febantel150.00/milligram(s)1.00Tablet
-
Praziquantel50.00/milligram(s)1.00Tablet
-
Pyrantel embonate144.00/milligram(s)1.00Tablet
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:
-
Luxembourg
Available in:
-
Luxembourg
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:
- Ministry Of Health And Social Security
Authorisation number:
- V 808/14/09/2160
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0338/001
Concerned member states:
-
Belgium
-
Czechia
-
Luxembourg
-
Slovakia
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: 26/08/2024
French (PDF)
Published on: 7/04/2025
Package Leaflet
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Labelling
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