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Fixed-dose combination

Dextrose, unspecified form, Potassium chloride and Sodium chloride

Also known as dextrose, unspecified form, potassium chloride, sodium chloride
Available on request
Presentations
6
Brands
0
Manufacturers
0
Available from stock
0

Dextrose, unspecified form, Potassium chloride and Sodium chloride is a fixed-dose combination of an osmotic laxative and a potassium salt. It is available as injection for intravenous use. MedsAcross supplies Dextrose, unspecified form, Potassium chloride and Sodium chloride for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Osmotic Laxative, Potassium Salt, Osmotic Activity, Increased Large Intestinal Motility, Inhibition Large Intestine Fluid/Electrolyte Absorption
US FDA first approval
Not recorded
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous
Dosage forms
Injection
Fixed-dose combination of
Dextrose, unspecified form, Potassium chloride, Sodium chloride

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

These intravenous solutions are indicated for use in adults and pediatric patients as sources of electrolytes, calories and water for hydration.

Source: US FDA prescribing information

Dosing overview

These solutions are for intravenous use only. Dosage is to be directed by a physician and is dependent upon age, weight, clinical condition of the patient and laboratory determinations. Frequent laboratory determinations and clinical evaluation are essential to monitor changes in blood glucose and electrolyte concentrations, and fluid and electrolyte balance during prolonged parenteral therapy. When a hypertonic solution is to be administered peripherally, it should be slowly infused through a small bore needle, placed well within the lumen of a large vein to minimize venous irritation. Carefully avoid infiltration. Usually, up to 40 mEq of potassium per liter daily is sufficient to replace normal loss in adults. Typical infusion rates should not exceed 10 mEq per hour or 120 mEq per day. Pediatric patients may require 2 to 3 mEq per kg of body weight daily.

Source: US FDA prescribing information

Contraindications

These solutions are contraindicated where the administration of sodium, potassium or chloride could be clinically detrimental. Solutions containing dextrose may be contraindicated in patients with hypersensitivity to corn products.

Source: US FDA prescribing information

Warnings and precautions

The administration of intravenous solutions can cause fluid and/or solute overload resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentration. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentration. Solutions containing sodium ions should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there is sodium retention with edema. In patients with diminished renal function, administration of solutions containing sodium or potassium ions may result in sodium or potassium retention.

Source: US FDA prescribing information

Side effects

Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia. Too rapid infusion of hypertonic solutions may cause local pain and venous irritation. Rate of administration should be adjusted according to tolerance. Use of the largest peripheral vein and a small bore needle is recommended. Symptoms may result from an excess or deficit of one or more of the ions present in the solution, therefore, frequent monitoring of electrolyte levels is essential. Hypernatremia may be associated with edema and exacerbation of congestive heart failure due to the retention of water, resulting in an expanded extracellular fluid volume.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

6 presentations of Dextrose, unspecified form, Potassium chloride and Sodium chloride, sorted by availability.

MedicineActive ingredientManufacturerRegisterAvailability
Dextrose, unspecified form, Potassium chloride and Sodium chloride 50 g/0.75 g/4.5 g per 1000 mL injectionIntravenousGeneric nameDextrose, unspecified form, Potassium chloride and Sodium chloride—US FDAAvailable on request
Dextrose, unspecified form, Potassium chloride and Sodium chloride 50 g/1.5 g/2 g per 1000 mL injectionIntravenousGeneric nameDextrose, unspecified form, Potassium chloride and Sodium chloride—US FDAAvailable on request
Dextrose, unspecified form, Potassium chloride and Sodium chloride 50 g/1.5 g/4.5 g per 1000 mL injectionIntravenousGeneric nameDextrose, unspecified form, Potassium chloride and Sodium chloride—US FDAAvailable on request
Dextrose, unspecified form, Potassium chloride and Sodium chloride 50 g/1.5 g/9 g per 1000 mL injectionIntravenousGeneric nameDextrose, unspecified form, Potassium chloride and Sodium chloride—US FDAAvailable on request
Dextrose, unspecified form, Potassium chloride and Sodium chloride 50 g/2.2 g/4.5 g per 1000 mL injectionIntravenousGeneric nameDextrose, unspecified form, Potassium chloride and Sodium chloride—US FDAAvailable on request
Dextrose, unspecified form, Potassium chloride and Sodium chloride 50 g/3 g/4.5 g per 1000 mL injectionIntravenousGeneric nameDextrose, unspecified form, Potassium chloride and Sodium chloride—US FDAAvailable on request

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDANot recorded—
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Dextrose, unspecified form, Potassium chloride and Sodium chloride available for export from India?

Yes, on request. MedsAcross lists 6 presentations of Dextrose, unspecified form, Potassium chloride and Sodium chloride and sources them for licensed hospitals, importers and physicians against valid import documents.

Does Dextrose, unspecified form, Potassium chloride and Sodium chloride need cold chain shipping?

No listed presentation of Dextrose, unspecified form, Potassium chloride and Sodium chloride is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

References

  1. Potassium Chloride in Dextrose and Sodium Chloride prescribing information (B. Braun Medical). U.S. National Library of Medicine, DailyMed. Retrieved 26 March 2024

Request Dextrose, unspecified form, Potassium chloride and Sodium chloride for export supply

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