Veterinary Medicines

HYPERSOL 500 MG/G POWDER FOR USE IN DRINKING WATER

Not authorised
  • Oxytetracycline hydrochloride
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Product identification

Medicine name:
HYPERSOL 500 MG/G POWDER FOR USE IN DRINKING WATER
HYPERSOL 500 mg/g POLVO PARA ADMINISTRACION EN AGUA DE BEBIDA
Active substance:
  • Oxytetracycline hydrochloride
Target species:
  • Chicken
  • Pig
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Oxytetracycline hydrochloride
    540.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • Oral use
    • Chicken
      • Eggs
        no withdrawal period
      • Meat and offal
        7
        day
    • Pig
      • Meat and offal
        7
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Spain
Package description:
  • 5 kg bucket: internal bag made of low density polyethylene (in contact with the veterinary medicinal product) in a bucket made of polypropylene – cover made of polypropylene
  • 5 kg : Bag made of low density polyethylene (in contact with the veterinary medicinal product) / paper / paper
  • 10 kg bags: Bag made of low density polyethylene (in contact with the veterinary medicinal product) / paper / paper
  • 1 kg jar: Jar made of high density polyethylene (in contact with the veterinary medicinal product) with a screw cap made of low density polyethylene / aluminium / cardboard operculum / polypropylene

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:
  • Huvepharma S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Huvepharma S.A.
Responsible authority:
  • (AEMPS)
Authorisation number:
  • 2740 ESP
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0251/001

Documents

Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 15/03/2023
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Summary of Product Characteristics

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Spanish (PDF)
Published on: 15/03/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 15/03/2023
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