Veterinary Medicines

Veloxa Forte Chewable Tablets for Dogs

Not authorised
  • Febantel
  • Pyrantel
  • Praziquantel
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Product identification

Medicine name:
Veloxa Forte Chewable Tablets for Dogs
Veloxa forte comprimidos mastigáveis para cães
Active substance:
  • Febantel
  • Pyrantel
  • Praziquantel
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Febantel
    525.00
    milligram(s)
    /
    1.00
    Tablet
  • Pyrantel
    175.00
    milligram(s)
    /
    1.00
    Tablet
  • Praziquantel
    175.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Chewable tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP52AA51
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Revoked
Authorised in:
  • Portugal
Package description:
  • PVC/Aluminium/Polyamide blister-forming laminate with aluminium lidding foil containing 2 chewable tablets. Box containing 1 blister strip of 2 chewable tablets (2 chewable tablets)
  • PVC/Aluminium/Polyamide blister-forming laminate with aluminium lidding foil containing 2 chewable tablets. Box containing 2 blister strips of 2 chewable tablets (4 chewable tablets)
  • PVC/Aluminium/Polyamide blister-forming laminate with aluminium lidding foil containing 2 chewable tablets. Box containing 4 blister strips of 2 chewable tablets (8 chewable tablets)
  • PVC/Aluminium/Polyamide blister-forming laminate with aluminium lidding foil containing 2 chewable tablets. Box containing 24 blister strips of 2 chewable tablets (48 chewable tablets)
  • PVC/Aluminium/Polyamide blister-forming laminate with aluminium lidding foil containing 2 chewable tablets. Box containing 48 blister strips of 2 chewable tablets (96 chewable tablets)

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:
  • Lavet Kft.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Lavet Kft.
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 591/02/12DFVPT
Date of authorisation status change:
Reference member state:
  • Hungary
Procedure number:
  • HU/V/0116/002