Caniphedrin 20 mg Tabletten für Hunde
Caniphedrin 20 mg Tabletten für Hunde
Authorised
- Ephedrine hydrochloride
Product identification
Medicine name:
Caniphedrin 20 mg Tabletten für Hunde
Caniphedrin 20 mg Tablet
Caniphedrin 20 mg Comprimé
Caniphedrin 20 mg Tablette
Active substance:
- Ephedrine hydrochloride
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Ephedrine hydrochloride20.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG04BX90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Heat-sealed blister pack, consisting of aluminium foil and a PVC foil with 10 tablets per blister. Package size: Cardboard box containing 10 blisters of 10 tablets each.
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:
- Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetviva Richter GmbH
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V573831
Date of authorisation status change:
Reference member state:
-
Austria
Procedure number:
- AT/V/0016/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Finland
-
France
-
Greece
-
Hungary
-
Italy
-
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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Labelling
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