Veterinary Medicine Information website

Solacyl 1000 mg/g powder for use in drinking water for turkeys

Authorised
  • Sodium salicylate
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Product identification

Medicine name:
Solacyl 1000 mg/g powder for use in drinking water for turkeys
Active substance:
  • Sodium salicylate
Target species:
  • Turkey
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Sodium salicylate
    1000.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • In drinking water use
    • Turkey
      • Egg
        no withdrawal period
      • Meat and offal
        2
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN02BA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Available in:
  • France
Package description:
  • (ID6) 5 kilogram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 5 kilogram(s)
  • (ID5) 2.5 kilogram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 2.5 kilogram(s)
  • (ID4) 1 kilogram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 1 kilogram(s)
  • (ID3) 500 gram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 500 gram(s)
  • (ID2) 250 gram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 250 gram(s)
  • (ID1) 100 gram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 100 gram(s)

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:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/1285829 7/2017
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0170/001
Concerned member states:
  • Czechia
  • France
  • Hungary
  • Italy
  • Netherlands
  • Poland
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 30/11/2023
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 15/10/2025
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Combined File of all Documents

English (PDF)
Published on: 12/01/2026
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2402381-paren-20171106.rtf

English (RTF)
Published on: 12/01/2026
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