Veterinary Medicines

OSMOLAR SOLUCION INYECTABLE

Not authorised
  • Calcium chloride dihydrate
  • Potassium chloride
  • Glucose monohydrate
  • Sodium chloride
  • Magnesium chloride hexahydrate
Download as PDF

Product identification

Medicine name:
OSMOLAR SOLUCION INYECTABLE
Active substance:
  • Calcium chloride dihydrate
  • Potassium chloride
  • Glucose monohydrate
  • Sodium chloride
  • Magnesium chloride hexahydrate
Target species:
  • Cattle (calf)
  • Sheep (lamb)
  • Pig (piglet)
Route of administration:
  • Subcutaneous use
  • Intravenous use

Product details

Active substance and strength:
  • Calcium chloride dihydrate
    0.37
    milligram(s)
    /
    1.00
    millilitre(s)
  • Potassium chloride
    0.74
    milligram(s)
    /
    1.00
    millilitre(s)
  • Glucose monohydrate
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium chloride
    4.90
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium chloride hexahydrate
    0.30
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle (calf)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep (lamb)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig (piglet)
      • Meat and offal
        0
        day
  • Intravenous use
    • Cattle (calf)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep (lamb)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig (piglet)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05BB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Spain
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • S P Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • S P Veterinaria S.A.
Responsible authority:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 3965 ESP
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.
Spanish (PDF)
Published on: 30/11/2023
Download

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 30/11/2023
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 30/11/2023
Download