AMODIP 1.25 MG CHEWABLE TABLETS FOR CATS
AMODIP 1.25 MG CHEWABLE TABLETS FOR CATS
Authorised
- Amlodipine besilate
Product identification
Medicine name:
AMODIP 1.25 MG CHEWABLE TABLETS FOR CATS
Amodip 1.25 mg Kauwtablet
Amodip 1.25 mg Comprimé à croquer
Amodip 1.25 mg Kautablette
Active substance:
- Amlodipine besilate
Target species:
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amlodipine besilate1.73/milligram(s)1.00Tablet
Pharmaceutical form:
-
Chewable tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QC08CA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Box containing 3 blister packs of 10 chewable tablets
- Box containing 20 blister packs of 10 chewable tablets
- Box containing 10 blister packs of 10 chewable tablets
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V505760
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0413/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
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
Documents
Package Leaflet
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Summary of Product Characteristics
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Labelling
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