Dronspot 30 mg/7.5 mg Spot-on Solution for Small Cats
Dronspot 30 mg/7.5 mg Spot-on Solution for Small Cats
Authorised
- Emodepside
- Praziquantel
Product identification
Medicine name:
Dronspot 30 mg/7.5 mg Spot-on Solution for Small Cats
Dronspot, 30/7,5mg, Roztok pro nakapání na kůži - spot-on
Active substance:
- Emodepside
- Praziquantel
Target species:
-
Cat
Route of administration:
-
Spot-on use
Product details
Active substance and strength:
-
Emodepside21.40milligram(s)1.00millilitre(s)
-
Praziquantel85.80milligram(s)1.00millilitre(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 subject to veterinary prescription except for some pack sizes
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Package description:
- White polypropylene pipettes with caps in aluminium blisters.Pack sizes: 0.35 ml per pipette.Blister packs containing 2 unit dose pipettes
- White polypropylene pipettes with caps in aluminium blisters.Pack sizes: 0.35 ml per pipette.Blister packs containing 1 unit dose pipettes.
- White polypropylene pipettes with caps in aluminium blisters.Pack sizes: 0.35 ml per pipette.Blister packs containing 20 units dose pipettes
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:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/039/19-C
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0310/001
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.
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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