Drontal Tasty Bone Wormer 150/144/50 mg tablets
Drontal Tasty Bone Wormer 150/144/50 mg tablets
Authorised
- Febantel
- Pyrantel embonate
- Praziquantel
Product identification
Medicine name:
Drontal Tasty Bone Wormer 150/144/50 mg tablets
Drontal Dog Flavour, 150/144/50mg, Tableta
Active substance:
- Febantel
- Pyrantel embonate
- Praziquantel
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Febantel150.00milligram(s)1.00Tablet
-
Pyrantel embonate144.00milligram(s)1.00Tablet
-
Praziquantel50.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AC55
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription except for some pack sizes
Authorisation status:
-
Valid
Authorised in:
-
Czechia
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:
- KVP Pharma+Veterinär Produkte GmbH
- EUROPHARTECH
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/077/15-C
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: 28/01/2022
Czech (PDF)
Published on: 25/10/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 25/10/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 25/10/2022
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