Veterinary Medicines

SELECTAN 300 mg/ml solution for injection for cattle and pigs

Authorised
  • Florfenicol
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Product identification

Medicine name:
SELECTAN 300 mg/ml solution for injection for cattle and pigs
SELECTAN 300 mg/ml Injektionslösung für Rinder und Schweine
Active substance:
  • Florfenicol
Target species:
  • Cattle
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Florfenicol
    300.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        30
        day
    • Pig
      • Meat and offal
        18
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01BA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:
  • Available only in German
  • Available only in German
  • Available only in German
  • Available only in German
  • Available only in German
  • Available only in German
  • Available only in German
  • The product is bottled in 100 ml colourless Type II glass bottle, closed with Type I polymeric elastomer stopper with aluminium cap.One bottle of 100 ml is available in a cardboard box.
  • The product is bottled in 100 ml colourless Type II glass bottle, closed with Type I polymeric elastomer stopper with aluminium cap.Clinical pack size:10 x 100 ml
  • The product is bottled in 100 ml colourless Type II glass bottle, closed with Type I polymeric elastomer stopper with aluminium cap.Clinical pack size:12 x 100 ml

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:
  • Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Hipra S.A.
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 8-00716
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0189/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 20/11/2025
Updated on: 22/12/2025
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Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
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German (PDF)
Published on: 20/11/2025
Updated on: 22/12/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 20/11/2025
Updated on: 22/12/2025
Download

Combined File of all Documents

English (PDF)
Published on: 28/09/2025
Download