Rapidol Sodium Bicarbonate Powder
NDC Package 55758-319-04

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

Package Information

Rapidol Sodium Bicarbonate (sodium bicarbonate) powders is do not take more than your “ maximum daily dosage for your age group” in a 24-hour period. This formulation utilizes a powder delivery system. Marketed by Pharmadel Llc, this product is identified by NDC 55758-319 and is authorized under FDA application M001.

Identification & Billing

NDC Package Code
55758-319-04
Package Description
113 g in 1 BOTTLE
Product Code
55758-319
11-Digit Billing Format
55758031904
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Rapidol Sodium Bicarbonate
Non-Proprietary Name
Sodium Bicarbonate
Substance Name
Sodium Bicarbonate
Dosage Form
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
SODIUM BICARBONATE 2.6 g/2.6g
Pharmacologic Class
Alkalinizing Activity - [MoA] (Mechanism of Action)
Usage Information
Do not take more than your “ maximum daily dosage for your age group” in a 24-hour period. See Warnings. take a ½ teaspoon in a 4 fl. oz. (½ a glass) of water every 2 hours up to the maximum daily dosage or as directed by a doctor dissolve completely in water before drinkingagemaximum daily dosageadults 60 years of age and over½ teaspoon, 3 times a dayadults under 60 and children 12 years of age and over½ teaspoon, 6 times a daychildren under 12 years of agedo not use

Regulatory & Marketing

Labeler Name
Pharmadel Llc
Product Type
Human Otc Drug
FDA Application #
M001
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-23-2020
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 55758-319-04 identifies a specific commercial package of 113 g in 1 bottle of Rapidol Sodium Bicarbonate, a human over the counter drug labeled by Pharmadel Llc. This powder 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 Pharmadel Llc on November 23, 2020. The current certification is valid through December 31, 2027.

How is this Pharmadel Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55758031904. 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)
55758-319-04
11-Digit CMS (5-4-2)
55758-0319-04

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