NDC Package 0904-7261-61 Sodium Bicarbonate

Tablet 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:
0904-7261-61
Package Description:
10 BLISTER PACK in 1 BOX, UNIT-DOSE / 10 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Sodium Bicarbonate
Non-Proprietary Name:
Sodium Bicarbonate
Substance Name:
Sodium Bicarbonate
Usage Information:
 do not use the maximum dosage for more than 2 weeks  tablets may be swallowed whole or dissolved in water prior to use  adults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tablets in 24 hours  adults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours
11-Digit NDC Billing Format:
00904726161
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
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:
    Major Pharmaceuticals
    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):
    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:
    10-26-2022
    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.

    Frequently Asked Questions

    What is NDC 0904-7261-61?

    The NDC Packaged Code 0904-7261-61 is assigned to a package of 10 blister pack in 1 box, unit-dose / 10 tablet in 1 blister pack of Sodium Bicarbonate, a human over the counter drug labeled by Major Pharmaceuticals. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0904-7261 included in the NDC Directory?

    Yes, Sodium Bicarbonate with product code 0904-7261 is active and included in the NDC Directory. The product was first marketed by Major Pharmaceuticals on October 26, 2022 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 0904-7261-61?

    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 10.

    What is the 11-digit format for NDC 0904-7261-61?

    The 11-digit format is 00904726161. 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 4-4-2 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
    4-4-20904-7261-615-4-200904-7261-61