Veterinary Medicines

Forthyron 800 Microgram Flavoured Tablet

Authorised
  • Levothyroxine sodium
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Product identification

Medicine name:
Forthyron 800 Microgram Flavoured Tablet
Forthyron flavoured 800 µg Tablet
Forthyron flavoured 800 µg Comprimé
Forthyron flavoured 800 µg Tablette
Active substance:
  • Levothyroxine sodium
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Levothyroxine sodium
    800.00
    microgram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH03AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • 10 tablets in a blister [Aluminium (20micrometre) - PVC_PE_PVDC (250_30_90) white], 25 blisters per carton
  • 10 tablets in a blister [Aluminium (20micrometre) - PVC_PE_PVDC (250_30_90) white], 5 blisters per carton

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Dales Pharmaceuticals Limited
  • Eurovet Animal Health B.V.
  • Genera d.d.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V415536
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0286/004
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 21/06/2022
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Summary of Product Characteristics

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Dutch (PDF)
Published on: 20/10/2025
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French (PDF)
Published on: 20/10/2025
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Package Leaflet

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Dutch (PDF)
Published on: 20/10/2025
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French (PDF)
Published on: 20/10/2025
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German (PDF)
Published on: 20/10/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 20/10/2025
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French (PDF)
Published on: 20/10/2025
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German (PDF)
Published on: 20/10/2025
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108736 - par.pdf

English (PDF)
Published on: 21/06/2022
Download