Sodium Bicarbonate 10 Gr Tablet
NDC Package 70795-1190-2

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

Package Information

Sodium Bicarbonate 10 Gr (sodium bicarbonate) tablets is adults: Take 1 tablet, dissolved in a glass of water, as needed. This formulation utilizes a tablet delivery system. Marketed by Graxcell Pharmaceutical, Llc, this product is identified by NDC 70795-1190 and is authorized under FDA application M001.

Identification & Billing

NDC Package Code
70795-1190-2
Package Description
200 TABLET in 1 BOTTLE
Product Code
70795-1190
11-Digit Billing Format
70795119002
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sodium Bicarbonate 10 Gr
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
Usage Information
Adults: Take 1 tablet, dissolved in a glass of water, as needed. Maxlmum daily dose for adults up to 60 years of age is 24 tablets. Maximum daily dose for adults 60 years of age or older is 12 tablets. Dissolve completely in water before drinking.D0 NOT EXCEED RECOMMENDED DOSENot recommended for children.

Regulatory & Marketing

Labeler Name
Graxcell Pharmaceutical, Llc
Product Type
Human Otc Drug
FDA Application #
M001
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-02-2017
Listing Expiration
12-31-2026
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (70795-1190). Click a package code to view its specific billing and regulatory data.

70795-1190-0
1000 TABLET in 1 BOTTLE
70795-1190-1
100 TABLET in 1 BOTTLE
70795-1190-5
500 TABLET in 1 BOTTLE

* 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 70795-1190-2 identifies a specific commercial package of 200 tablet in 1 bottle of Sodium Bicarbonate 10 Gr, a human over the counter drug labeled by Graxcell Pharmaceutical, 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 Graxcell Pharmaceutical, Llc on October 02, 2017. The current certification is valid through December 31, 2026.

How is this Graxcell Pharmaceutical, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70795119002. 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 (5-4-1)
70795-1190-2
11-Digit CMS (5-4-2)
70795-1190-02

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