Sodium Bicarbonate 10 Gr. (650 Mg) Tablet
NDC Package 77333-829-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Sodium Bicarbonate 10 Gr. (650 Mg) (sodium bicarbonate) tablets is do not use the maximum dosage for more than 2 weekstablets may be swallowed whole or dissolved in water prior to useadults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tablets in 24 hoursadults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours. This formulation utilizes a tablet delivery system. Marketed by Gendose Pharmaceuticals, Llc, this product is identified by NDC 77333-829 and is authorized under FDA application M001.

Identification & Billing

NDC Package Code
77333-829-10
Package Description
100 BLISTER PACK in 1 BOX, UNIT-DOSE / 10 TABLET in 1 BLISTER PACK (77333-829-25)
Product Code
77333-829
11-Digit Billing Format
77333082910
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sodium Bicarbonate 10 Gr. (650 Mg)
Non-Proprietary Name
Sodium Bicarbonate
Substance Name
Sodium Bicarbonate
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
SODIUM BICARBONATE 650 mg/1
Pharmacologic Class
Alkalinizing Activity - [MoA] (Mechanism of Action)
Usage Information
Do not use the maximum dosage for more than 2 weekstablets may be swallowed whole or dissolved in water prior to useadults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tablets in 24 hoursadults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours

Regulatory & Marketing

Labeler Name
Gendose Pharmaceuticals, Llc
Product Type
Human Otc Drug
FDA Application #
M001
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-01-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 77333-829-10 identifies a specific commercial package of 100 blister pack in 1 box, unit-dose / 10 tablet in 1 blister pack (77333-829-25) of Sodium Bicarbonate 10 Gr. (650 Mg), a human over the counter drug labeled by Gendose Pharmaceuticals, Llc. This tablet is formulated for oral use and contains sodium bicarbonate 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 Gendose Pharmaceuticals, Llc on May 01, 2026. The current certification is valid through December 31, 2027.

How is this Gendose Pharmaceuticals, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 77333082910. 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 (5-3-2)
77333-829-10
11-Digit CMS (5-4-2)
77333-0829-10

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