Dronspot 60 mg/15 mg Spot-on Solution for Medium Cats
Dronspot 60 mg/15 mg Spot-on Solution for Medium Cats
Authorised
- Praziquantel
- Emodepside
Product identification
Medicine name:
Dronspot 60 mg/15 mg Spot-on Solution for Medium Cats
Dronspot 60 mg / 0,70 ml + 15 mg / 0,70 ml Roztwór do nakrapiania
Active substance:
- Praziquantel
- Emodepside
Target species:
-
Cat
Route of administration:
-
Spot-on use
Product details
Active substance and strength:
-
Praziquantel60.00milligram(s)0.70millilitre(s)
-
Emodepside15.00milligram(s)0.70millilitre(s)
Pharmaceutical form:
-
Spot-on solution
Withdrawal period by route of administration:
-
Spot-on use
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AA51
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- White polypropylene pipettes with caps in aluminium blisters. Pack sizes: 0.70 ml per pipette. Blister packs containing 20 unit dose pipettes
- White polypropylene pipettes with caps in aluminium blisters. Pack sizes: 0.70 ml per pipette. Blister packs containing 2 unit dose pipettes.
- White polypropylene pipettes with caps in aluminium blisters. Pack sizes: 0.70 ml per pipette. Blister packs containing 1 unit dose pipette.
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+Veterinaer Produkte GmbH
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2893
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0310/002
Concerned member states:
-
Belgium
-
Czechia
-
Finland
-
Hungary
-
Italy
-
Luxembourg
-
Poland
-
Slovakia
-
Sweden
-
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.
Polish (PDF)
Published on: 16/01/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 26/03/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 7/02/2023
How useful was this page?: