Potassium Acetate Injection, Solution, Concentrate
NDC Package 0409-3294-25

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Potassium Acetate injection is uSP (2 mEq/mL) is indicated as a source of potassium, for the addition to large volume intravenous fluids, to prevent or correct hypokalemia in patients with restricted or no oral intake. This formulation utilizes a injection, solution, concentrate delivery system. Marketed by Hospira, Inc., this product is identified by NDC 0409-3294 and is authorized under FDA application NDA018896.

Identification & Billing

NDC Package Code
0409-3294-25
Package Description
25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-3294-15)
Product Code
0409-3294
11-Digit Billing Format
00409329425
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Potassium Acetate
Non-Proprietary Name
Potassium Acetate
Substance Name
Potassium Acetate
Dosage Form
Injection, Solution, Concentrate - A sterile preparation for parenteral use which, upon the addition of suitable solvents, yields a solution conforming in all respects to the requirements for Injections.
Administration Route
  • Intravenous - Administration within or into a vein or veins.
  • Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Potassium Acetate Injection, USP (2 mEq/mL) is indicated as a source of potassium, for the addition to large volume intravenous fluids, to prevent or correct hypokalemia 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.

Regulatory & Marketing

Labeler Name
Hospira, Inc.
Product Type
Human Prescription Drug
FDA Application #
NDA018896
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
12-23-2013
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0409-3294). Click a package code to view its specific billing and regulatory data.

0409-3294-51
25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-3294-61)

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0409-3294-25 identifies a specific commercial package of 25 vial, pharmacy bulk package in 1 tray / 50 ml in 1 vial, pharmacy bulk package (0409-3294-15) of Potassium Acetate, a human prescription drug labeled by Hospira, Inc.. This injection, solution, concentrate is formulated for intravenous use and contains potassium acetate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Hospira, Inc. on December 23, 2013. The current certification is valid through December 31, 2027.

How is this Hospira, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00409329425. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (4-4-2)
0409-3294-25
11-Digit CMS (5-4-2)
00409-3294-25

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.