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  5. NDC Package Code: 52682-206-04 Sodium Bicarbonate

NDC Package 52682-206-04 Sodium Bicarbonate

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

Table of Contents

    1. Package Information
    2. 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:
52682-206-04
Package Description:
1000 TABLET in 1 BOTTLE, PLASTIC
Product Code:
52682-206
Proprietary Name:
Sodium Bicarbonate
Non-Proprietary Name:
Sodium Bicarbonate
Substance Name:
Sodium Bicarbonate
Usage Information:
Relieves:acid indigestionheartburnsour stomachupset stomachassociated with these symptoms
11-Digit NDC Billing Format:
52682020604
NDC to RxNorm Crosswalk:
  • RxCUI: 198861 - sodium bicarbonate 650 MG Oral Tablet
  • RxCUI: 198861 - NaHCO3 650 MG Oral Tablet
  • RxCUI: 198861 - sodium bicarbonate 10 Grains Oral Tablet
  • RxCUI: 198861 - sodium bicarbonate 648 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Ingenus Pharmaceuticals Nj, Llc
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • SODIUM BICARBONATE 650 mg/1
    • Pharmacologic Class(es):
  • Alkalinizing Activity - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    part331
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    01-24-2011
    End Marketing Date:
    04-01-2025
    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.

    Frequently Asked Questions

    What is NDC 52682-206-04?

    The NDC Packaged Code 52682-206-04 is assigned to a package of 1000 tablet in 1 bottle, plastic of Sodium Bicarbonate, a human over the counter drug labeled by Ingenus Pharmaceuticals Nj, Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 52682-206 included in the NDC Directory?

    Yes, Sodium Bicarbonate with product code 52682-206 is active and included in the NDC Directory. The product was first marketed by Ingenus Pharmaceuticals Nj, Llc on January 24, 2011.

    What is the 11-digit format for NDC 52682-206-04?

    The 11-digit format is 52682020604. 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
    5-3-252682-206-045-4-252682-0206-04