Otomicol ear drops and cutaneous suspension for dogs, cats and guinea pigs
Otomicol ear drops and cutaneous suspension for dogs, cats and guinea pigs
Authorised
- Miconazole nitrate
- Prednisolone acetate
- POLYMYXIN B SULFATE
Product identification
Medicine name:
Otomicol ear drops and cutaneous suspension for dogs, cats and guinea pigs
Active substance:
- Miconazole nitrate
- Prednisolone acetate
- POLYMYXIN B SULFATE
Target species:
-
Cat
-
Dog
-
Guinea pig
Route of administration:
-
Auricular use
-
Cutaneous use
Product details
Active substance and strength:
-
Miconazole nitrate23.00/milligram(s)1.00millilitre(s)
-
Prednisolone acetate5.00/milligram(s)1.00millilitre(s)
-
POLYMYXIN B SULFATE5500.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Ear drops, suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QS02CA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- (ID1) 15 millilitre(s): Box (Cardboard) with 1 Bottle (Low Density PolyEthylene) with 15 millilitre(s), closed with Tropfer and Verschluss mit Originalitätssicherung (Low Density PolyEthylene, High Density PolyEthylene)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application – bioavailability studies cannot be used to demonstrate bioequivalence (Article 19(1)(b) of Regulation (EU) 2019/6)
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:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V663137
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0342/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Croatia
-
Czechia
-
Estonia
-
France
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Labelling
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Package Leaflet
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Combined File of all Documents
English (PDF)
Download Published on: 13/03/2026
7014442-paren-20240508.pdf
English (PDF)
Download Published on: 13/03/2026