NDC Package 70010-021-01 Potassium Chloride Extended Release

Potassium Chloride Tablet, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
70010-021-01
Package Description:
100 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Potassium Chloride Extended Release
Non-Proprietary Name:
Potassium Chloride
Substance Name:
Potassium Chloride
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.
11-Digit NDC Billing Format:
70010002101
NDC to RxNorm Crosswalk:
  • RxCUI: 312529 - potassium chloride 8 MEQ (600 MG) Extended Release Oral Tablet
  • RxCUI: 312529 - potassium chloride 8 MEQ Extended Release Oral Tablet
  • RxCUI: 312529 - K+ Chloride 8 MEQ Extended Release Oral Tablet
  • RxCUI: 312529 - Pot Chloride 8 MEQ Extended Release Oral Tablet
  • RxCUI: 312529 - potassium chloride 600 MG Extended Release Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Granules Pharmaceuticals Inc.
    Dosage Form:
    Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA211797
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-22-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70010-021-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE
    70010-021-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE
    70010-021-613 BLISTER PACK in 1 CARTON / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    70010-021-6210 BLISTER PACK in 1 CARTON / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70010-021-01?

    The NDC Packaged Code 70010-021-01 is assigned to a package of 100 tablet, extended release in 1 bottle of Potassium Chloride Extended Release, a human prescription drug labeled by Granules Pharmaceuticals Inc.. The product's dosage form is tablet, extended release and is administered via oral form.

    Is NDC 70010-021 included in the NDC Directory?

    Yes, Potassium Chloride Extended Release with product code 70010-021 is active and included in the NDC Directory. The product was first marketed by Granules Pharmaceuticals Inc. on October 22, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70010-021-01?

    The 11-digit format is 70010002101. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-270010-021-015-4-270010-0021-01