Prinovox 40 mg + 10 mg spot-on solution for small dogs
Prinovox 40 mg + 10 mg spot-on solution for small dogs
Authorised
- Moxidectin
- Imidacloprid
Product identification
Medicine name:
Prinovox 40 mg + 10 mg spot-on solution for small dogs
Prinovox 40 mg + 10 mg Lösung zum Auftropfen für kleine Hunde
Active substance:
- Moxidectin
- Imidacloprid
Target species:
-
Dog
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Moxidectin10.00milligram(s)0.40millilitre(s)
-
Imidacloprid40.00milligram(s)0.40millilitre(s)
Pharmaceutical form:
-
Spot-on solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AB52
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- (ID6): 1 unspecified outer container with 21 Pipette (PolyPropylene) with 0.4 millilitre(s) (8.4 millilitre(s))
- (ID5): 1 unspecified outer container with 6 Pipette (PolyPropylene) with 0.4 millilitre(s) (2.4 millilitre(s))
- (ID4): 1 unspecified outer container with 4 Pipette (PolyPropylene) with 0.4 millilitre(s) (1.6 millilitre(s))
- (ID3): 1 unspecified outer container with 3 Pipette (PolyPropylene) with 0.4 millilitre(s) (1.2 millilitre(s))
- (ID2): 1 unspecified outer container with 2 Pipette (PolyPropylene) with 0.4 millilitre(s) (0.8 millilitre(s))
- (ID1): 1 unspecified outer container with 1 Pipette (PolyPropylene) with 0.4 millilitre(s) (0.4 millilitre(s))
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:
- Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- KVP Pharma+Veterinaer Produkte GmbH
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402351.00.00
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0196/003
Concerned member states:
-
Ireland
-
Italy
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 14/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 4/11/2024
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 4/11/2024
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