MedPath
HSA Product

10 mEq Potassium Chloride in 5% Dextrose and 0.33% Sodium Chloride Injection, USP

Product approved by Health Sciences Authority (SG)

Basic Information

10 mEq Potassium Chloride in 5% Dextrose and 0.33% Sodium Chloride Injection, USP

INJECTION

Regulatory Information

SIN13224P

November 28, 2006

General Sale List

Therapeutic

INTRAVENOUS

January 24, 2024

May 30, 2025

XB05BB01

Company Information

BAXTER HEALTHCARE (ASIA) PTE LTD

BAXTER HEALTHCARE (ASIA) PTE LTD

Active Ingredients

Sodium Chloride

Strength: 3.3 g/L

Potassium Chloride

Strength: 1.5 g/L

Dextrose Hydrous

Strength: 50 g/L

Detailed Information

Contraindications

**4 CONTRAINDICATIONS** Potassium Chloride in Dextrose and Sodium Chloride Injection is contraindicated in patients with: - known hypersensitivity to potassium chloride, dextrose and/or sodium chloride _\[see Warnings and Precautions 5.1) – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information\]_ - clinically significant hyperkalemia _\[see Warnings and Precautions (5.2) – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information\]_ - clinically significant hyperglycemia _\[see Warnings and Precautions (5.3) – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information\]_

Indication Information

**1 INDICATIONS AND USAGE** Potassium Chloride in Dextrose and Sodium Chloride Injection is indicated as a source of water, electrolytes and calories.

© Copyright 2025. All Rights Reserved by MedPath