Eliminall 402 mg spot-on solution for dogs
Eliminall 402 mg spot-on solution for dogs
Not authorised
- Fipronil
Product identification
Medicine name:
Eliminall 402 mg spot-on solution for dogs
ELIMINALL 402 mg SOLUCION PARA UNCION DORSAL PUNTUAL PARA PERROS
Active substance:
- Fipronil
Target species:
-
Dog
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Fipronil402.00/milligram(s)4.02millilitre(s)
Pharmaceutical form:
-
Spot-on solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AX15
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Spain
Package description:
- (ID6) 3618 millilitre(s): Box (Cardboard) with 30 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 30 Pipette (PolyPropylene) each with 4.02 millilitre(s)
- (ID5) 1608 millilitre(s): Box (Cardboard) with 20 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 20 Pipette (PolyPropylene) each with 4.02 millilitre(s)
- (ID4) 402 millilitre(s): Box (Cardboard) with 10 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 10 Pipette (PolyPropylene) each with 4.02 millilitre(s)
- (ID3) 144.72 millilitre(s): Box (Cardboard) with 6 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 6 Pipette (PolyPropylene) each with 4.02 millilitre(s)
- (ID2) 36.18 millilitre(s): Box (Cardboard) with 3 Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) each with 3 Pipette (PolyPropylene) each with 4.02 millilitre(s)
- (ID1) 4.02 millilitre(s): Box (Cardboard) with Beutel (Low Density PolyEthylene; PolyEthylene TerePhthalate; Aluminium) with 1 Pipette (PolyPropylene) with 4.02 millilitre(s)
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:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 2408 ESP
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0189/005
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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