Fungiderm 0,005 g/ml roztwór dla koni, lisów, psów, kotów, świnek morskich, myszy, szczurów i królików
Fungiderm 0,005 g/ml roztwór dla koni, lisów, psów, kotów, świnek morskich, myszy, szczurów i królików
Authorised
- Clotrimazole
Product identification
Medicine name:
Fungiderm 0,005 g/ml roztwór dla koni, lisów, psów, kotów, świnek morskich, myszy, szczurów i królików
Active substance:
- Clotrimazole
Target species:
-
Rat
-
Mouse
-
Dog
-
Rabbit
-
Fox
-
Cat
-
Horse
-
Guinea pig
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Clotrimazole0.01/gram(s)1.00millilitre(s)
Pharmaceutical form:
-
Cutaneous solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Rat
-
All relevant tissuesno withdrawal periodNot applicable.
-
-
Mouse
-
All relevant tissuesno withdrawal periodNot applicable.
-
-
Dog
-
Rabbit
-
Not applicable0day
-
-
Fox
-
All relevant tissuesno withdrawal periodNot applicable.
-
-
Cat
-
Horse
-
Not applicable0dayDo not use in horses whose tissues are intended for human consumption. Horses treated with the product must be identified as not intended for human consumption in the animal treatment book and on the identification document (passport) accompanying registered equines.
-
-
Guinea pig
-
All relevant tissuesno withdrawal periodNot applicable.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD01AC01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Biowet Drwalew Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Drwalewskie Zaklady Przemyslu Bioweterynaryjnego S.A.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0767
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 16/01/2025
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 16/01/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 16/01/2025
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