Veterinary Medicine Information website

Enrotron 100 mg/ml oral solution for chicken and turkeys

Authorised
  • Enrofloxacin
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Product identification

Medicine name:
Enrotron 100 mg/ml oral solution for chicken and turkeys
Active substance:
  • Enrofloxacin
Target species:
  • Turkey
  • Rabbit
  • Chicken
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Enrofloxacin
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Turkey
      • Meat and offal
        13
        day
    • Rabbit
      • Meat and offal
        15
        day
    • Chicken
      • Meat and offal
        7
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01MA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Available in:
  • Poland
Package description:
  • Cardboard box containing 6 x 1000 ml opaque polyethylene bottle with opaque polyethylene tamper evident screw cap and polypropylene measuring pitcher.
  • Cardboard box containing 12 x 100 ml opaque polyethylene bottle with opaque polyethylene tamper evident screw cap and polypropylene measuring pitcher.
  • 1000 ml opaque polyethylene bottle with opaque polyethylene tamper evident screw cap and polypropylene measuring pitcher
  • Cardboard box containing 100 ml opaque polyethylene bottle with opaque polyethylene tamper evident screw cap and polypropylene measuring pitcher.

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:
  • aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • aniMedica GmbH
  • Industrial Veterinaria S.A.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 2312
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0165/003
Concerned member states:
  • Cyprus
  • France
  • Germany
  • Ireland
  • Poland
  • United Kingdom (Northern Ireland)

Documents

Labelling

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Polish (PDF)
Published on: 4/02/2022
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Summary of Product Characteristics

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Polish (PDF)
Published on: 4/02/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/02/2022
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