Veterinary Medicines

SODIUM SALICYL 80% WSP, powder for oral solution for cattle (calves) and pig

Authorised
  • Sodium salicylate
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Product identification

Medicine name:
SODIUM SALICYL 80% WSP, powder for oral solution for cattle (calves) and pig
Sodium Salicyl 80% WSP
Active substance:
  • Sodium salicylate
Target species:
  • Cattle (calf)
  • Pig
Route of administration:
  • In drinking water/milk use

Product details

Active substance and strength:
  • Sodium salicylate
    800.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • In drinking water/milk use
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN02BA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:
  • 1 kg composite can. Composite can: container consisting of PET/aluminium/adhesive/paper, with a PET/aluminium tear-off membrane and a HDPE lid.
  • 1 kg bucket. Bucket: polypropylene bucket provided with a polypropylene lid.
  • 5 kg bucket. Bucket: polypropylene bucket provided with a polypropylene lid.
  • 2,5 kg bucket. Bucket: polypropylene bucket provided with a polypropylene lid.
  • Securitainer: white polypropylene cylindrical container provided with a low-density polyethylene lid. The securitainer contains 1 kg of product.

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:
  • Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Dopharma B.V.
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 401257.00.00
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0133/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Poland
  • Portugal
  • Romania
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 19/03/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 20/12/2024
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 20/12/2024
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NL V 133 001 DC Sodium salicyl 80 WSP PuAR_updated 082021.pdf

English (PDF)
Published on: 19/03/2024
Download