Veterinary Medicines

PRURIVET N, Kožní roztok

Authorised
  • Chloramphenicol
  • Dexamethasone
  • Benzyl benzoate
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Product identification

Medicine name:
PRURIVET N, Kožní roztok
Active substance:
  • Chloramphenicol
  • Dexamethasone
  • Benzyl benzoate
Target species:
  • Dog
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Chloramphenicol
    12.00
    milligram(s)
    /
    1.00
    gram(s)
  • Dexamethasone
    0.50
    milligram(s)
    /
    1.00
    gram(s)
  • Benzyl benzoate
    100.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Cutaneous solution
Withdrawal period by route of administration:
  • Cutaneous use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QD07CB04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Vetoquinol s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol Biowet Sp. z o.o.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/069/03-C
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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