DEXTROSE- dextrose monohydrate injection, solution 
Fresenius Kabi USA, LLC


5% Dextrose Injection, USP


Rx only


5% Dextrose Injection, USP solution is sterile and nonpyrogenic.  It is a parenteral solution containing dextrose in water for injection intended for intravenous administration.

Each 100 mL of 5% Dextrose Injection, USP, contains dextrose monohydrate, 5 g in water for injection.  The caloric value is 170 kcal/L.  The osmolarity is 252 mOsmol/L (calc.), which is slightly hypotonic.

The solution pH is 4.3 (3.2 to 6.5).

This solution contains no bacteriostat, antimicrobial agent or added buffer and is intended only as a single-dose injection.  When smaller doses are required the unused portion should be discarded.

5% Dextrose Injection, USP is a parenteral fluid and nutrient replenisher.

Dextrose, USP is chemically designated D-glucose monohydrate (C 6H 12O 6 • H 2O), a hexose sugar freely soluble in water.  It has the following structural formula:          


Water for Injection, USP is chemically designated H 2O.

The flexible container is fabricated from a specially formulated non-plasticized film containing polypropylene and thermoplastic elastomers ( freeflex® bag).  The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly.  Solutions in contact with the flexible container can leach out certain of the container’s chemical components in very small amounts within the expiration period.  The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.


When administered intravenously, these solutions provide a source of water and carbohydrate.

Isotonic and hypertonic concentrations of dextrose are suitable for parenteral maintenance of water requirements when salt is not needed or should be avoided.

Solutions containing carbohydrate in the form of dextrose restore blood glucose levels and provide calories.  Carbohydrate in the form of dextrose may aid in minimizing liver glycogen depletion and exerts a protein-sparing action.  Dextrose injected parenterally undergoes oxidation to carbon dioxide and water.

Water is an essential constituent of all body tissues and accounts for approximately 70% of total body weight.  Average normal adult daily requirements range from two to three liters (1 to 1.5 liters each for insensible water loss by perspiration and urine production).

Water balance is maintained by various regulatory mechanisms.  Water distribution depends primarily on the concentration of electrolytes in the body compartments and sodium (Na +) plays a major role in maintaining physiologic equilibrium.


Intravenous solutions containing dextrose are indicated for parenteral replenishment of fluid and minimal carbohydrate calories as required by the clinical condition of the patient.


5% Dextrose Injection, USP without electrolytes should not be administered simultaneously with blood through the same infusion set because of the possibility that pseudoagglutination of red cells may occur.


Excessive administration of potassium-free solutions may result in significant hypokalemia.

The intravenous administration of these solutions can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema.

The risk of dilutional states is inversely proportional to the electrolyte concentrations of administered parenteral solutions.  The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of such solutions.


Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid balance, electrolyte concentrations and acid-base balance during prolonged parenteral therapy or whenever the condition of the patient warrants such evaluation.

Solutions containing dextrose should be used with caution in patients with known subclinical or overt diabetes mellitus.

Do not administer unless solution is clear and container is undamaged.  Discard unused portion.

Carcinogenesis, Mutagenesis, Impairment of Fertility

Studies with 5% Dextrose Injection, USP have not been performed to evaluate carcinogenic potential, mutagenic potential or effects on fertility.


Teratogenic Effects

Pregnancy Category C . Animal reproduction studies have not been conducted with dextrose.  It is also not known whether dextrose can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.  Dextrose should be given to a pregnant woman only if clearly needed.

Nursing Mothers

Caution should be exercised when 5% Dextrose Injection, USP is administered to a nursing mother.

Pediatric Use

The safety and effectiveness in the pediatric population are based on the similarity of the clinical conditions of the pediatric and adult populations.  In neonates or very small infants the volume of fluid may affect fluid and electrolyte balance.

Frequent monitoring of serum glucose concentrations is required when dextrose is prescribed to pediatric patients, particularly neonates and low birth weight infants.

In very low birth weight infants, excessive or rapid administration of dextrose injection may result in increased serum osmolarity and possible intracerebral hemorrhage.

Geriatric Use

An evaluation of current literature revealed no clinical experience identifying differences in response between elderly and younger patients.  In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.


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.

If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary.


In the event of overhydration or solute overload, re-evaluate the patient and institute appropriate corrective measures (see WARNINGS,  PRECAUTIONS, and ADVERSE REACTIONS).


The dose is dependent upon the age, weight and clinical condition of the patient.

As reported in the literature, the dosage and constant infusion rate of intravenous dextrose must be selected with caution in pediatric patients, particularly neonates and low birth weight infants, because of the increased risk of hyperglycemia/hypoglycemia.

Drug Interactions

Additives may be incompatible.  Consult with pharmacist, if available.  When introducing additives, use aseptic technique, mix thoroughly and do not store.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit (see PRECAUTIONS).


Check flexible container solution composition, lot number, and expiry date.

Do not remove solution container from its overwrap until immediately before use.

Use sterile equipment and aseptic technique.

To Open

1. Turn solution container over so that the text is face down. Using the pre-cut corner tabs, peel open the overwrap and remove solution container.

2. Check the solution container for leaks by squeezing firmly. If leaks are found, or if the seal is not intact, discard the solution.

3. Do not use if the solution is cloudy or a precipitate is present.

To Add Medication

1. Identify WHITE Additive Port with arrow pointing toward container.

2. Immediately before injecting additives, break off WHITE Additive Port Cap with the arrow pointing toward container.

3. Hold base of WHITE Additive Port horizontally.

4. Insert needle horizontally through the center of WHITE Additive Port’s septum and inject additives.

5. Mix container contents thoroughly.

Preparation for Administration

1. Immediately before inserting the infusion set, break off BLUE Infusion Port Cap with the arrow pointing away from container.

2. Use a non-vented infusion set or close the air-inlet on a vented set.

3. Close the roller clamp of the infusion set.

4. Hold the base of BLUE Infusion Port.

5. Insert spike through BLUE Infusion Port by rotating wrist slightly until the spike is inserted.

NOTE: See full directions accompanying administration set.

WARNING: Do not use flexible container in series connections.


5% Dextrose Injection, USP is supplied in single dose flexible plastic containers as follows:

Product CodeUnit of SaleStrengthEach
624650 NDC 63323-624-50
Package of 60 freeflex® bags
2.5 grams per 50 mL
(50 mg per mL)
NDC 63323-624-05
50mL fill in a 100 mL freeflex® Bag
624661 NDC 63323-624-61
Package of 50 freeflex® bags
5 grams per 100 mL
(50 mg per mL)
NDC 63323-624-06
One 100 mL freeflex® Bag
624674 NDC 63323-624-74
Package of 30 freeflex® bags
12.5 grams per 250 mL
(50 mg per mL)
NDC 63323-624-04
One 250 mL freeflex® Bag
624675 NDC 63323-624-75
Package of 20 freeflex® bags
25 grams per 500 mL
(50 mg per mL)
NDC 63323-624-07
One 500 mL freeflex® Bag
624610 NDC 63323-624-10
Package of 10 freeflex® bags
50 grams per 1,000 mL
(50 mg per mL)
NDC 63323-624-03
One 1,000 mL freeflex® Bag

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

Exposure of pharmaceutical products to heat should be minimized.  Avoid excessive heat.  Protect from freezing.

The container closure is not made with natural rubber latex.  Non-PVC, Non-DEHP, Sterile.

Manufactured for:
Lake Zurich, IL 60047

Revised: December 2018

5% Dextrose Injection, USP NDC 63323-624-06
5 grams per 100 mL 

(50 mg per mL)
For intravenous use.      Rx only

dextrose monohydrate injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:63323-624
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63323-624-5060 in 1 CASE07/31/2018
1NDC:63323-624-0550 mL in 1 BAG; Type 0: Not a Combination Product
2NDC:63323-624-6150 in 1 CASE10/21/2016
2NDC:63323-624-06100 mL in 1 BAG; Type 0: Not a Combination Product
3NDC:63323-624-7430 in 1 CASE10/21/2016
3NDC:63323-624-04250 mL in 1 BAG; Type 0: Not a Combination Product
4NDC:63323-624-7520 in 1 CASE10/21/2016
4NDC:63323-624-07500 mL in 1 BAG; Type 0: Not a Combination Product
5NDC:63323-624-1010 in 1 CASE10/21/2016
5NDC:63323-624-031000 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Labeler - Fresenius Kabi USA, LLC (608775388)
NameAddressID/FEIBusiness Operations
Fresenius Kabi Deutschland GmbH506719546ANALYSIS(63323-624) , MANUFACTURE(63323-624)
NameAddressID/FEIBusiness Operations
HP Halden Pharma AS347747373ANALYSIS(63323-624) , PACK(63323-624) , MANUFACTURE(63323-624)

Revised: 4/2024
Document Id: 40c07bed-7ccc-4117-a595-78c2a053e8a9
Set id: f2379398-a07b-417e-a022-f7b41f962067
Version: 7
Effective Time: 20240424
Fresenius Kabi USA, LLC