BOB MARTIN VETCARE SPOT ON FIPRONIL 134 MG SOLUTION SPOT-ON FOR MEDIUM DOGS
BOB MARTIN VETCARE SPOT ON FIPRONIL 134 MG SOLUTION SPOT-ON FOR MEDIUM DOGS
Authorised
- Fipronil
Product identification
Medicine name:
BOB MARTIN VETCARE SPOT ON FIPRONIL 134 MG SOLUTION SPOT-ON FOR MEDIUM DOGS
Kruidvat vlooiendruppels 134 mg oplossing voor middelgrote honden
Active substance:
- Fipronil
Target species:
-
Dog
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Fipronil134.00/milligram(s)1.00Pipette
Pharmaceutical form:
-
Spot-on solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AX15
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Package description:
- Carton box of one blister of 2 pipettes of 1,34 mL
- Carton box of one blister of 3 pipettes of 1,34 mL
- Carton box of one blister of 4 pipettes of 1,34 mL
- Carton box of one blister of 5 pipettes of 1,34 mL
- Carton box of one blister of 6 pipette1 of 1,34 mL
- Blister card of one blister of 1 pipette of 1,34 mL
- Blister card of one blister of 2 pipettes of 1,34 mL
- Blister card of one blister of 3 pipettes of 1,34 mL
- Blister card of one blister of 4 pipettes of 1,34 mL
- Blister card of one blister of 5 pipettes of 1,34 mL
- Blister card of one blister of 6 pipettes of 1,34 mL
- Carton box of one blister of 1 pipette of 1,34 mL
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Pets Choice Healthcare Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Baggerman Farmanet N.V.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 119213
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0427/003
Concerned member states:
-
Italy
-
Netherlands
-
Poland
-
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: 24/03/2022