Potassium Chloride Injection, Solution
NDC Package 63323-669-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Potassium Chloride (potassium chloride, dextrose monohydrate) injection is a medication a mineral supplement used to treat or prevent low amounts of potassium in the blood. This formulation utilizes a injection, solution delivery system. Marketed by Fresenius Kabi Usa, Llc, this product is identified by NDC 63323-669 and is authorized under FDA application ANDA212346.

Identification & Billing

NDC Package Code
63323-669-10
Package Description
10 BAG in 1 CASE / 1000 mL in 1 BAG (63323-669-01)
Product Code
11-Digit Billing Format
63323066910
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk
  • RxCUI: 2566844 - potassium chloride 10 MEQ / dextrose 5 % in 1000 ML Injection
  • RxCUI: 2566844 - 1000 ML dextrose monohydrate 50 MG/ML / potassium chloride 0.01 MEQ/ML Injection
  • RxCUI: 2566844 - 1000 ML dextrose monohydrate 50 MG/ML / K+ chloride 0.01 MEQ/ML Injection
  • RxCUI: 2566844 - 1000 ML dextrose monohydrate 50 MG/ML / Pot chloride 0.01 MEQ/ML Injection
  • RxCUI: 2566844 - potassium chloride 10 MEQ / dextrose 5 % per 1000 ML Injection

Clinical Specifications

Proprietary Name
Potassium Chloride
Non-Proprietary Name
Potassium Chloride, Dextrose Monohydrate
Substance Name
Dextrose Monohydrate; Potassium Chloride
Dosage Form
Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
Administration Route
Intravenous - Administration within or into a vein or veins.
Usage Information
This medication is a mineral supplement used to treat or prevent low amounts of potassium in the blood. A normal level of potassium in the blood is important. Potassium helps your cells, kidneys, heart, muscles, and nerves work properly. Most people get enough potassium by eating a well-balanced diet. Some conditions that can lower your body's potassium level include severe prolonged diarrhea and vomiting, hormone problems such as hyperaldosteronism, or treatment with "water pills"/diuretics.

Regulatory & Marketing

Labeler Name
Fresenius Kabi Usa, Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA212346
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
04-23-2021
Listing Expiration
12-31-2026
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.

Billing & HCPCS Mapping

To facilitate insurance claims and reimbursement, this drug package is mapped to specific HCPCS administrative codes. This crosswalk aligns clinical data with the billing standards used in ASP (Average Sales Price), AWP, and OPPS payment systems. Use the cards below to identify the correct billable units for provider claims.

Source: ASP
Inj potassium chloride
HCPCS Dosage 2 MEQ
Units / Pkg 100

Note for Medical Coders: These mappings are synthesized from various CMS datasets including OPPS, PrEP, and DAC (Data Analysis and Coding) contractors. Always confirm unit conversions against the current quarter's pricing files before final submission.

* 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 63323-669-10 identifies a specific commercial package of 10 bag in 1 case / 1000 ml in 1 bag (63323-669-01) of Potassium Chloride, a human prescription drug labeled by Fresenius Kabi Usa, Llc. This injection, solution is formulated for intravenous use and contains dextrose monohydrate; potassium chloride 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 Fresenius Kabi Usa, Llc on April 23, 2021. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

This medication is a mineral supplement used to treat or prevent low amounts of potassium in the blood. A normal level of potassium in the blood is important. Potassium helps your cells, kidneys, heart, muscles, and nerves work properly. Most people get enough potassium by eating a well-balanced diet. Some conditions that can lower your body's potassium level include severe prolonged diarrhea and vomiting, hormone problems such as hyperaldosteronism, or treatment with "water pills"/diuretics.

How is this Fresenius Kabi Usa, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63323066910. 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 (5-3-2)
63323-669-10
11-Digit CMS (5-4-2)
63323-0669-10

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