FOR ADDITIVE USE ONLY AFTER DILUTION IN INTRAVENOUS FLUIDS.

Rx only

Sodium acetate injection USP, 40 mEq (2 mEq/mL) is a sterile, nonpyrogenic, concentrated solution of sodium acetate in water for injection. The solution is administered, after dilution, by the intravenous route as an electrolyte replenisher. It must not be administered undiluted. Each 20 mL contains 3.28 g of sodium acetate (anhydrous) which provides 40 mEq each of sodium (Na+) and acetate (CH3COO−). The solution contains no bacteriostat, antimicrobial agent or added buffer. May contain acetic acid for pH adjustment; the pH is 6.5 (6.0 to 7.0). The osmolar concentration is 4 mOsmol/mL (calc); specific gravity 1.081.

The solution is intended as an alternative to sodium chloride to provide sodium ion (Na+) for addition to large volume infusion fluids for intravenous use.

Sodium Acetate, USP (anhydrous) is chemically designated CH3COONa, a hygroscopic powder very soluble in water.

Sodium is the principal cation of extracellular fluid. It comprises more than 90% of total cations at its normal plasma concentration of approximately 140 mEq/liter. The sodium ion exerts a primary role in controlling total body water and its distribution.

Acetate (CH3COO−), a source of hydrogen ion acceptors, is an alternate source of bicarbonate (HCO3−) by metabolic conversion in the liver. This conversion has been shown to proceed readily, even in the presence of severe liver disease.

Sodium acetate injection 40 mEq is indicated as a source of sodium, for addition to large volume intravenous fluids to prevent or correct hyponatremia in patients with restricted or no oral intake. It is also useful as an additive for preparing specific intravenous fluid formulas when the needs of the patient cannot be met by standard electrolyte or nutrient solutions.

Sodium acetate injection 40 mEq is contraindicated in patients with hypernatremia or fluid retention.

Sodium acetate injection 40 mEq must be diluted before use.

To avoid sodium overload and water retention, infuse sodium-containing solutions slowly.

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 exists edema with sodium retention.

In patients with diminished renal function, administration of solutions containing sodium ions may result in sodium retention.

Solutions containing acetate ions should be used with great care in patients with metabolic or respiratory alkalosis. Acetate should be administered with great care in those conditions in which there is an increased level or an impaired utilization of this ion, such as severe hepatic insufficiency.

The intravenous administration of this solution (after appropriate dilution) can cause fluid and/or solute overloading resulting in dilution of other serum electrolyte concentrations, overhydration, congested states or pulmonary edema. Excessive administration of potassium free solutions may result in significant hypokalemia.

WARNING: This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.

Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.

Sodium overload can occur with intravenous infusion of excessive amounts of sodium-containing solutions. (see WARNINGS and PRECAUTIONS).

In the event of overdosage, discontinue infusion containing sodium acetate immediately and institute corrective therapy as indicated to reduce elevated serum sodium levels, and restore acid-base balance if necessary. (see WARNINGS, PRECAUTIONS and ADVERSE REACTIONS).

Sodium acetate injection 40 mEq is administered intravenously only after dilution in a larger volume of fluid. The dose and rate of administration are dependent upon the individual needs of the patient. Serum sodium should be monitored as a guide to dosage. Using aseptic technique, all or part of the contents of one or more vials may be added to other intravenous fluids to provide any desired number of milliequivalents (mEq) of sodium (Na+) with an equal number of acetate (CH3COO−).

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

Sodium acetate injection USP, 40 mEq (2 mEq/mL) is supplied as follows:

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

Distributed by

Hikma Pharmaceuticals USA Inc.

Berkeley Heights, NJ 07922

Revised December 2023

462-972-02

NDC 0641-6261-01 Rx only

Sodium Acetate Injection, USP

40 mEq per 20 mL

(2 mEq/mL)

CAUTION: MUST BE DILUTED

For Intravenous Use

20 mL Single-Dose Vial

Discard unused portion

NDC 0641-6261-01 Rx only

Sodium Acetate Injection, USP

40 mEq per 20 mL

(2 mEq/mL)

CAUTION: MUST BE DILUTED

For Intravenous Use

1 x 20 mL Single-Dose Vial