Veterinary Medicines

Ossitetraciclina 20% Chemifarma, 200 mg/g Polvere solubile per soluzione orale per polli da carne, tacchini, galline ovaiole, conigli, suini, vitelli da latte

Authorised
  • Oxytetracycline
Download as PDF

Product identification

Medicine name:
Ossitetraciclina 20% Chemifarma, 200 mg/g Polvere solubile per soluzione orale per polli da carne, tacchini, galline ovaiole, conigli, suini, vitelli da latte
Ossitetraciclina 20% Chemifarma, 200 mg/g Polvere solubile per soluzione orale per polli da carne, tacchini, galline ovaiole, conigli, suini, vitelli da latte
Active substance:
  • Oxytetracycline
Target species:
  • Chicken (broiler)
  • Turkey
  • Chicken (layer hen)
  • Pig
  • Rabbit
  • Cattle (suckling calf)
Route of administration:
  • In drinking water/milk use

Product details

Active substance and strength:
  • Oxytetracycline
    200.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water/milk
Withdrawal period by route of administration:
  • In drinking water/milk use
    • Chicken (broiler)
      • Meat and offal
        7
        day
    • Turkey
      • Meat and offal
        12
        day
    • Chicken (layer hen)
      • Egg
        5
        day
    • Pig
      • Meat and offal
        12
        day
    • Rabbit
      • Meat and offal
        12
        day
    • Cattle (suckling calf)
      • Meat and offal
        20
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
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:
  • Chemifarma S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Chemifarma - S.p.A.
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 9/12/2022
Download
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."