Veterinary Medicines

Centidox 100%, powder for use in drinking water or milk/milk replacer for calves and pigs

Authorised
  • Doxycycline hyclate
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Product identification

Medicine name:
Centidox 100%, powder for use in drinking water or milk/milk replacer for calves and pigs
CENTIDOX 1000 mg/g POLVO PARA ADMINISTRACION EN AGUA DE BEBIDA O EN LECHE (LACTORREEMPLAZANTE) PARA BOVINO Y PORCINO
Active substance:
  • Doxycycline hyclate
Target species:
  • Cattle (calf)
  • Pig
Route of administration:
  • In drinking water/milk use

Product details

Active substance and strength:
  • Doxycycline hyclate
    1000.00
    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
    • Cattle (calf)
      • Meat and offal
        16
        day
    • Pig
      • Meat and offal
        8
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Spain
Package description:
  • 250 g alufoil sachets in a carton box. Sachet with outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • 100 g alufoil sachets in a carton box. Sachet with outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • 500 g alufoil sachets in a carton box. Sachet with outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • 10 x 100 g alufoil sachets in a carton box. Sachet with outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • 1 kg alufoil sachets in a carton box. Sachet with outside a white layer, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
  • 250 g alufoil sachets in a carton box. Sachet with an outer layer of polyester, middle layers of polyethylene and aluminium and an inner layer of an ionomer (Surlyn).
  • 100 g alufoil sachets in a carton box. Sachet with an outer layer of polyester, middle layers of polyethylene and aluminium and an inner layer of an ionomer (Surlyn).
  • 500 g alufoil sachets in a carton box. Sachet with an outer layer of polyester, middle layers of polyethylene and aluminium and an inner layer of an ionomer (Surlyn).
  • 1 kg alufoil sachets in a carton box. Sachet with an outer layer of polyester, middle layers of polyethylene and aluminium and an inner layer of an ionomer (Surlyn).
  • 10 x 100 g alufoil sachets in a carton box. Sachet with an outer layer of polyester, middle layers of polyethylene and aluminium and an inner layer of an ionomer (Surlyn).
  • 250 g alufoil sachets in a carton box.Sachet with an outer layer of polyethylene terephtalic acid, middle layers of aluminium and polyamide and an inner layer of polyethylene.
  • 100 g alufoil sachets in a carton box.Sachet with an outer layer of polyethylene terephtalic acid, middle layers of aluminium and polyamide and an inner layer of polyethylene.
  • 500 g alufoil sachets in a carton box.Sachet with an outer layer of polyethylene terephtalic acid, middle layers of aluminium and polyamide and an inner layer of polyethylene.
  • 1 kg alufoil sachets in a carton box.Sachet with an outer layer of polyethylene terephtalic acid, middle layers of aluminium and polyamide and an inner layer of polyethylene.
  • 10 x 100 g alufoil sachets in a carton box.Sachet with an outer layer of polyethylene terephtalic acid, middle layers of aluminium and polyamide and an inner layer of polyethylene.

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:
  • Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Responsible authority:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 2209 ESP
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0142/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • Denmark
  • Germany
  • Italy
  • Poland
  • Slovakia
  • Spain

Documents

Summary of Product Characteristics

English (PDF)
Published on: 19/11/2025
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Spanish (PDF)
Published on: 6/11/2025
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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: 6/11/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 6/11/2025
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Package Leaflet and Labelling

English (PDF)
Published on: 19/11/2025
Download