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D-glucose

Generic Name
D-glucose
Brand Names
As 3, Cpda-1 Blood Collection System, Dextrose and Electrolyte No. 75, Dianeal Low Calcium 1.5, Dianeal Pd-2/1.5, Ionosol-MB, Isolyte P, Leukotrap, Normosol-M, Plasma-lyte 148 In 5 % Dextrose, Prismasol
Drug Type
Small Molecule
Chemical Formula
C6H12O6
CAS Number
50-99-7
Unique Ingredient Identifier
5SL0G7R0OK

Overview

Glucose is a simple sugar (monosaccharide) generated during phosynthesis involving water, carbon and sunlight in plants. It is produced in humans via hepatic gluconeogenesis and breakdown of polymeric glucose forms (glycogenolysis). It circulates in human circulation as blood glucose and acts as an essential energy source for many organisms through aerobic or anaerobic respiration and fermentation. It is primarily stored as starch in plants and glycogen in animals to be used in various metabolic processes in the cellular level. Its aldohexose stereoisomer, dextrose or D-glucose, is the most commonly occurring isomer of glucose in nature. L-glucose is a synthesized enantiomer that is used as a low-calorie sweetener and laxative. The unspecified form of glucose is commonly supplied as an injection for nutritional supplementation or metabolic disorders where glucose levels are improperly regulated. Glucose is listed on the World Health Organization's List of Essential Medicines, the most important medications needed in a basic health system.

Indication

Glucose pharmaceutical formulations (oral tablets, injections) are indicated for caloric supply and carbohydrate supplementation in case of nutrient deprivation. It is also used for metabolic disorders such as hypoglycemia.

Associated Conditions

  • Dehydration
  • End-stage Chronic Kidney Failure
  • Fluid Loss
  • Hypoglycemia
  • Local Anaesthesia therapy
  • Potassium imbalance

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Haemonetics Corporation
57826-455
EXTRACORPOREAL
464 mg in 1 mL
9/30/2020
QOL Medical, LLC
67871-007
INTRATHECAL
8 mg in 10 mL
3/20/2012
Lukare Medical, LLC
55792-007
INTRATHECAL
8 mg in 10 mL
11/16/2018
Haemonetics Corporation
57826-460
EXTRACORPOREAL
100 mg in 1 mL
9/11/2020

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
DIANEAL PD-2 PERITONEAL DIALYSIS SOLUTION WITH 4.25% DEXTROSE
SIN05589P
SOLUTION, STERILE
4.25 g/100 ml
3/27/1991
DIANEAL LOW CALCIUM (2.5 mEq/l) PERITONEAL DIALYSIS SOLUTION WITH 1.5% DEXTROSE
SIN06627P
SOLUTION, STERILE
1.5 g/100 ml
10/14/1991
DEXTROSE INJECTION USP 70%
SIN10166P
INJECTION
70 g/100 ml
10/6/1998
DIANEAL PD-2 PERITONEAL DIALYSIS SOLUTION WITH 1.5% DEXTROSE
SIN05590P
SOLUTION, STERILE
1.5 g/100 ml
3/27/1991
DEXTROSE 5% AND SODIUM CHLORIDE 0.2% INJECTION USP
SIN05730P
INJECTION
5 g/100 ml
4/8/1991
PERIOLIMEL N4E Emulsion for Infusion
SIN16888P
EMULSION
75.0g/L
10/20/2023
OLIMEL N9E Emulsion for Infusion
SIN16890P
EMULSION
110.0g/L
10/20/2023
10 mEq Potassium Chloride in 5% Dextrose and 0.33% Sodium Chloride Injection, USP
SIN13224P
INJECTION
50 g/L
11/28/2006
DEXTROSE 5% AND SODIUM CHLORIDE 0.9% INJECTION USP
SIN05731P
INJECTION
5 g/100 ml
4/8/1991
DIANEAL LOW CALCIUM (2.5 mEq/l) PERITONEAL DIALYSIS SOLUTION WITH 4.25% DEXTROSE
SIN06625P
SOLUTION, STERILE
4.25 g/100 ml
10/14/1991

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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