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Veterinary Medicines

Kefavet® vet. 500 mg, film-coated tablet

Authorised
  • Cefalexin monohydrate

Product identification

Medicine name:
Kefavet® vet. 500 mg, film-coated tablet
Kefavet vet 500 mg filmomhulde tabletten
Active substance:
  • Cefalexin monohydrate
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Cefalexin monohydrate
    526.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Film-coated tablet
Withdrawal period by route of administration:
  • Oral use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01DB01
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • Blister, 28 tablets
  • Blister, 140 tablets
  • Blister, 70 tablets
  • Blister, 14 tablets
  • Blister, 30 tablets

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Orion Corporation
Marketing authorisation date:
Manufacturing sites for batch release:
  • Orion Corporation
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 106753
Date of authorisation status change:
Reference member state:
  • Sweden
Procedure number:
  • SE/V/0114/002
Concerned member states:
  • Belgium
  • Czechia
  • Denmark
  • Estonia
  • Hungary
  • Iceland
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Romania
  • Slovakia
  • Slovenia

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 5/04/2022
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