Dermanolon 1.77 mg/ml + 17.7 mg/ml cutaneous spray, solution for dogs and cats
Dermanolon 1.77 mg/ml + 17.7 mg/ml cutaneous spray, solution for dogs and cats
Authorised
- Triamcinolone acetonide
- Salicylic acid
Product identification
Medicine name:
Dermanolon 1.77 mg/ml + 17.7 mg/ml cutaneous spray, solution for dogs and cats
Active substance:
- Triamcinolone acetonide
- Salicylic acid
Target species:
-
Dog
-
Cat
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Triamcinolone acetonide2.00milligram(s)1.00millilitre(s)
-
Salicylic acid20.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Cutaneous spray, solution
Withdrawal period by route of administration:
-
Cutaneous use
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD07XB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Carton containing one 75 ml white, high density polyethylene container with spray pump and a styrene acrylonitrile polymer cap.
- Carton containing one 50 ml white, high density polyethylene container with spray pump and a styrene acrylonitrile polymer cap.
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:
- Le Vet. Beheer B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Produlab Pharma B.V.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10475/026/001
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0205/001
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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