Veterinary Medicines

Actikor 20 mg Film-coated Tablets for Dogs

Not authorised
  • Benazepril hydrochloride
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Product identification

Medicine name:
Actikor 20 mg Film-coated Tablets for Dogs
Actikor
Active substance:
  • Benazepril hydrochloride
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Benazepril hydrochloride
    20.00
    milligram(s)
    /
    1.00
    Piece
Pharmaceutical form:
  • Film-coated tablet
Withdrawal period by route of administration:
  • Oral use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QC09AA07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Sweden
Package description:
  • 14 tablets in aluminium foil blister packs
  • 84 tablets in aluminium foil blister packs
  • 56 tablets in aluminium foil blister packs
  • 28 tablets in aluminium foil blister packs
  • 140 tablets in aluminium foil blister packs

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:
  • Ecuphar
Marketing authorisation date:
Manufacturing sites for batch release:
  • Accord Healthcare Limited
  • Ecuphar
Responsible authority:
  • Swedish Medical Products Agency
Authorisation number:
  • 44446
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0151/002
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