Potassium Chloride Tablet, Film Coated, Extended Release
NDC Package 70518-2964-3

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 Chloride tablets is a medication a mineral supplement used to treat or prevent low amounts of potassium in the blood. This formulation utilizes a tablet, film coated, extended release delivery system. Marketed by Remedyrepack Inc., this product is identified by NDC 70518-2964 and is authorized under FDA application ANDA210921.

Identification & Billing

NDC Package Code
70518-2964-3
Package Description
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code
70518-2964
11-Digit Billing Format
70518296403
RxNorm Crosswalk
  • RxCUI: 628953 - potassium chloride 10 MEQ (750 MG) Extended Release Oral Tablet
  • RxCUI: 628953 - potassium chloride 10 MEQ Extended Release Oral Tablet
  • RxCUI: 628953 - K+ Chloride 10 MEQ Extended Release Oral Tablet
  • RxCUI: 628953 - Pot Chloride 10 MEQ Extended Release Oral Tablet
  • RxCUI: 628953 - potassium chloride 750 MG (potassium 10 mEq) Extended Release Oral Tablet

Clinical Specifications

Proprietary Name
Potassium Chloride
Non-Proprietary Name
Potassium Chloride
Substance Name
Potassium Chloride
Dosage Form
Tablet, Film Coated, Extended Release - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
POTASSIUM CHLORIDE 750 mg/1
Pharmacologic Class
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
Remedyrepack Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA210921
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
12-09-2020
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 (70518-2964). Click a package code to view its specific billing and regulatory data.

70518-2964-0
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
70518-2964-1
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
70518-2964-2
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
70518-2964-4
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

* 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 70518-2964-3 identifies a specific commercial package of 90 tablet, film coated, extended release in 1 bottle, plastic of Potassium Chloride, a human prescription drug labeled by Remedyrepack Inc.. This tablet, film coated, extended release is formulated for oral use and contains 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 Remedyrepack Inc. on December 09, 2020. The current certification is valid through December 31, 2027.

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 Remedyrepack Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70518296403. 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 (5-4-1)
70518-2964-3
11-Digit CMS (5-4-2)
70518-2964-03

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