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  5. NDC Package Code: 69452-193-20 Potassium Citrate

NDC Package 69452-193-20 Potassium Citrate

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
69452-193-20
Package Description:
100 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
69452-193
Proprietary Name:
Potassium Citrate
Non-Proprietary Name:
Potassium Citrate
Substance Name:
Potassium Citrate
Usage Information:
This medication is used to make the urine less acidic. This effect helps the kidneys get rid of uric acid, thereby helping to prevent gout and kidney stones. This medication can also prevent and treat certain metabolic problems (acidosis) caused by kidney disease. Citric acid and citrate salts (which contain potassium and sodium) belong to a class of drugs known as urinary alkalinizers. If you have a condition that requires you to limit your intake of potassium and sodium, your doctor may direct you to take a product that is lower in potassium and sodium.
11-Digit NDC Billing Format:
69452019320
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 199381 - potassium citrate 10 MEQ Extended Release Oral Tablet
  • RxCUI: 199381 - K+ citrate 10 MEQ Extended Release Oral Tablet
  • RxCUI: 199381 - Pot citrate 10 MEQ Extended Release Oral Tablet
  • RxCUI: 199381 - potassium citrate 1080 MG Extended Release Oral Tablet
  • RxCUI: 898490 - potassium citrate 15 MEQ Extended Release Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bionpharma 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):
  • POTASSIUM CITRATE 10 meq/1
    • Pharmacologic Class(es):
  • Acidifying Activity - [MoA] (Mechanism of Action)
  • Anti-coagulant - [EPC] (Established Pharmacologic Class)
  • Calcium Chelating Activity - [MoA] (Mechanism of Action)
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    ANDA212799
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-14-2019
    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
    69452-193-30500 TABLET, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69452-193-20?

    The NDC Packaged Code 69452-193-20 is assigned to a package of 100 tablet, extended release in 1 bottle of Potassium Citrate, a human prescription drug labeled by Bionpharma Inc.. The product's dosage form is tablet, extended release and is administered via oral form.

    Is NDC 69452-193 included in the NDC Directory?

    Yes, Potassium Citrate with product code 69452-193 is active and included in the NDC Directory. The product was first marketed by Bionpharma Inc. on December 14, 2019 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 NDC billing unit for package 69452-193-20?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 100.

    What is the 11-digit format for NDC 69452-193-20?

    The 11-digit format is 69452019320. 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
    5-3-269452-193-205-4-269452-0193-20