DERMIPRED 5 MG TABLETS FOR DOGS
DERMIPRED 5 MG TABLETS FOR DOGS
Authorised
- Prednisolone
Product identification
Medicine name:
DERMIPRED 5 MG TABLETS FOR DOGS
Dermipred 5,0 mg Tabletka
Active substance:
- Prednisolone
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Prednisolone5.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Available in:
-
Poland
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:
- Ceva Animal Health Polska Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2649
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0301/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Czechia
-
Denmark
-
Finland
-
Germany
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Slovakia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
Package Leaflet
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in another language below.
Polish (PDF)
Published on: 4/02/2022
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: 4/02/2022
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