Veterinary Medicines

Sureseal 2.6 g Intramammary Suspension for Cattle

Authorised
  • Bismuth subnitrate, heavy
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Product identification

Medicine name:
Sureseal 2.6 g Intramammary Suspension for Cattle
SURESEAL 2,6 G SUSPENSION INTRAMAMMAIRE POUR BOVINS
Active substance:
  • Bismuth subnitrate, heavy
Target species:
  • Cattle
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • Bismuth subnitrate, heavy
    2.60
    gram(s)
    /
    1.00
    Syringe
Pharmaceutical form:
  • Intramammary suspension
Withdrawal period by route of administration:
  • Intramammary use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG52X
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:
  • Low density polyethylene syringe with a smooth tapered hermetically sealed nozzle.Pack sizes:Buckets of 120 syringes including 120 individually wrapped teat cleaning towels
  • Low density polyethylene syringe with a smooth tapered hermetically sealed nozzle.Pack sizes:Cartons of 60 syringes including 60 individually wrapped teat cleaning towels
  • Low density polyethylene syringe with a smooth tapered hermetically sealed nozzle.Pack sizes:Cartons of 24 syringes including 24 individually wrapped teat cleaning towels

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:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Laboratories Limited
  • Norbrook Manufacturing Limited
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/8378076 5/2013
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0586/001
Concerned member states:
  • Belgium
  • France
  • Italy
  • Netherlands
  • Portugal
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 26/01/2025
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French (PDF)
Published on: 19/03/2025
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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: 26/01/2025
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