Veterinary Medicines Information website

SODIUM CHLORIDE OSALIA 0.9% SOLUTION FOR INJECTION OR INFUSION FOR CATTLE, HORSES,PIGS, SHEEP, GOATS, DOGS AND CATS

Authorised
  • Sodium chloride
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Product identification

Medicine name:
SODIUM CHLORIDE OSALIA 0.9% SOLUTION FOR INJECTION OR INFUSION FOR CATTLE, HORSES,PIGS, SHEEP, GOATS, DOGS AND CATS
Active substance:
  • Sodium chloride
Target species:
  • Cattle
  • Pig
  • Cat
  • Equid
  • Horse
  • Sheep
  • Goat
  • Dog
Route of administration:
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Sodium chloride
    9.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection/infusion
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Equid
      • Milk
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Equid
      • Milk
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05BB01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Estonia
Package description:
  • Box of 1 vial of 100 ml
  • Box of 2 bags of 5000 ml
  • Box of 1 bag of 5000 ml
  • Box of 5 bags of 2000 ml
  • Box of 1 bag of 2000 ml
  • Box of 10 bags of 1000 ml
  • Box of 1 bag of 1000 ml
  • Box of 12 vials of 500 ml
  • Box of 1 vial of 500 ml
  • Box of 20 vials of 250 ml
  • Box of 1 vial of 250 ml
  • Box of 30 vials of 100 ml

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:
  • Osalia
Marketing authorisation date:
Manufacturing sites for batch release:
  • S.A.L.F. S.p.A. Laboratorio Farmacologico
Responsible authority:
  • State Agency Of Medicines
Authorisation number:
  • 1273926
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0443/001
Concerned member states:
  • Estonia
  • Latvia
  • Lithuania
  • Romania

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Estonian (PDF)
Published on: 26/10/2026
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Estonian (PDF)
Published on: 26/10/2026
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Estonian (PDF)
Published on: 26/10/2026
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