Skip to main content
Veterinary Medicines

Genoxytab F, 1g, Intrauterine tablet

Authorised
  • Oxytetracycline hydrochloride

Product identification

Medicine name:
Genoxytab F, 1g, Intrauterine tablet
Genoxytab F, 1 g, comprimate intrauterine pentru vaci
Active substance:
  • Oxytetracycline hydrochloride
Target species:
  • Cattle (cow)
Route of administration:
  • Intrauterine use

Product details

Active substance and strength:
  • Oxytetracycline hydrochloride
    1.00
    gram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Intrauterine tablet
Withdrawal period by route of administration:
  • Intrauterine use
    • Cattle (cow)
      • Meat and offal
        7
        day
      • Milk
        5
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG51AA01
Authorisation status:
  • Valid
Authorised in:
  • Romania
Package description:
  • Plastic Bag 100 x 1.0 Tablet
  • Plastic Bag 40 x 1.0 Tablet
  • Plastic Bag 10 x 1.0 Tablet

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Genera d.d.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Genera d.d.
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 220047
Date of authorisation status change:
Reference member state:
  • Czechia
Procedure number:
  • CZ/V/0130/001
Concerned member states:
  • Bulgaria
  • Hungary
  • Romania

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Romanian (PDF)
Published on: 8/03/2022

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Romanian (PDF)
Published on: 23/03/2022
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."