Veterinary Medicines

Caniphedrin 50 mg Tabletten für Hunde

Authorised
  • Ephedrine hydrochloride
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Product identification

Medicine name:
Caniphedrin 50 mg Tabletten für Hunde
Caniphedrin 50 mg tabletten voor honden
Active substance:
  • Ephedrine hydrochloride
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Ephedrine hydrochloride
    50.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG04BX90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Available in:
  • Netherlands
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:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 125856
Date of authorisation status change:
Reference member state:
  • Austria
Procedure number:
  • AT/V/0016/002
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)

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 26/05/2025
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Summary of Product Characteristics

English (PDF)
Published on: 21/01/2025
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