Prinovox 100 mg + 25 mg spot-on solution for medium dogs
Prinovox 100 mg + 25 mg spot-on solution for medium dogs
Authorised
- Moxidectin
- Imidacloprid
Product identification
Medicine name:
Prinovox 100 mg + 25 mg spot-on solution for medium dogs
Prinovox 100 mg + 25 mg solução para unção punctiforme para cães médios
Active substance:
- Moxidectin
- Imidacloprid
Target species:
-
Dog
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Moxidectin25.00milligram(s)1.00millilitre(s)
-
Imidacloprid100.00milligram(s)1.00millilitre(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:
-
Portugal
Package description:
- (ID6): 1 unspecified outer container with 21 Pipette (PolyPropylene) with 1 millilitre(s) (21 millilitre(s))
- (ID5): 1 unspecified outer container with 6 Pipette (PolyPropylene) with 1 millilitre(s) (6 millilitre(s))
- (ID4): 1 unspecified outer container with 4 Pipette (PolyPropylene) with 1 millilitre(s) (4 millilitre(s))
- (ID3): 1 unspecified outer container with 3 Pipette (PolyPropylene) with 1 millilitre(s) (3 millilitre(s))
- (ID2): 1 unspecified outer container with 2 Pipette (PolyPropylene) with 1 millilitre(s) (2 millilitre(s))
- (ID1): 1 unspecified outer container with 1 Pipette (PolyPropylene) with 1 millilitre(s) (1 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 Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- KVP Pharma+Veterinaer Produkte GmbH
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 1091/04/17RFVPT
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0196/004
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
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Published on: 15/11/2024
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