Potassium Phosphate Injection, Solution
NDC Package 70069-746-25

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

Package Information

Potassium Phosphate injection is potassium phosphates injection is indicated as a source of phosphorus:in intravenous fluids to correct hypophosphatemia in adults and pediatric patients when oral or enteral replacement is not possible, insufficient or contraindicated.for parenteral nutrition in adults and pediatric patients when oral or enteral nutrition is not possible, insufficient or contraindicated. This formulation utilizes a injection, solution delivery system. Marketed by Somerset Therapeutics, Llc, this product is identified by NDC 70069-746 and is authorized under FDA application ANDA217726.

Identification & Billing

NDC Package Code
70069-746-25
Package Description
25 BOTTLE in 1 CARTON / 5 mL in 1 BOTTLE
Product Code
70069-746
11-Digit Billing Format
70069074625
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk
  • RxCUI: 1928567 - potassium phosphates (phosphorus 15 MMOL / potassium 22 MEQ) in 5 ML Injection
  • RxCUI: 1928567 - 5 ML dibasic potassium phosphate 236 MG/ML / monobasic potassium phosphate 224 MG/ML Injection
  • RxCUI: 1928567 - 5 ML Dibasic K+ phosphate 236 MG/ML / Monobasic K+ phosphate 224 MG/ML Injection
  • RxCUI: 1928567 - 5 ML Dibasic Pot phosphate 236 MG/ML / Monobasic Pot phosphate 224 MG/ML Injection
  • RxCUI: 1928567 - phosphorus 15 MMOL / potassium 22 MEQ per 5 ML Injection

Clinical Specifications

Proprietary Name
Potassium Phosphate
Non-Proprietary Name
Potassium Phosphate
Substance Name
Dibasic Potassium Phosphate; Monobasic Potassium Phosphate
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.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Potassium phosphates injection is indicated as a source of phosphorus:in intravenous fluids to correct hypophosphatemia in adults and pediatric patients when oral or enteral replacement is not possible, insufficient or contraindicated.for parenteral nutrition in adults and pediatric patients when oral or enteral nutrition is not possible, insufficient or contraindicated.

Regulatory & Marketing

Labeler Name
Somerset Therapeutics, Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA217726
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-11-2024
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70069-746-25 identifies a specific commercial package of 25 bottle in 1 carton / 5 ml in 1 bottle of Potassium Phosphate, a human prescription drug labeled by Somerset Therapeutics, Llc. This injection, solution is formulated for intravenous use and contains dibasic potassium phosphate; monobasic potassium phosphate 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 Somerset Therapeutics, Llc on July 11, 2024. The current certification is valid through December 31, 2026.

How is this Somerset Therapeutics, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70069074625. 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)
70069-746-25
11-Digit CMS (5-4-2)
70069-0746-25

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