Veterinary Medicines

CHLORURE DE SODIUM OSALIA 0,9 % SOLUTION INJECTABLE OU POUR PERFUSION POUR BOVINS, CHEVAUX, PORCS, OVINS, CAPRINS, CHIENS ET CHATS

Authorised
  • Sodium chloride
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Product identification

Medicine name:
CHLORURE DE SODIUM OSALIA 0,9 % SOLUTION INJECTABLE OU POUR PERFUSION POUR BOVINS, CHEVAUX, PORCS, OVINS, CAPRINS, CHIENS ET CHATS
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
    • Cat
    • 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
    • Dog
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Cat
    • 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
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05BB01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:

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:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/4058207 8/2019
Date of authorisation status change:

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: 11/12/2024
Download

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: 11/12/2024
Download
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