Drontal Tasty Bone Multi-worm XL 525/504/175 mg tablets
Drontal Tasty Bone Multi-worm XL 525/504/175 mg tablets
Authorised
- Febantel
- Pyrantel embonate
- Praziquantel
Product identification
Medicine name:
Drontal Tasty Bone Multi-worm XL 525/504/175 mg tablets
Drontal Dog Flavour XL 525/504/175 mg δισκία
Active substance:
- Febantel
- Pyrantel embonate
- Praziquantel
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Febantel525.00milligram(s)1.00Tablet
-
Pyrantel embonate504.00milligram(s)1.00Tablet
-
Praziquantel175.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AA51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
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 8 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 48 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
Responsible authority:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
- CY00687V
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0337/002
Concerned member states:
-
Bulgaria
-
Croatia
-
Cyprus
-
Estonia
-
Greece
-
Hungary
-
Latvia
-
Lithuania
-
Poland
-
Portugal
-
Romania
-
Slovenia
-
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: 3/05/2024
Greek (PDF)
Published on: 19/05/2022
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