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  5. NDC Package Code: 55758-319-04 Rapidol Sodium Bicarbonate

NDC Package 55758-319-04 Rapidol Sodium Bicarbonate

Sodium Bicarbonate Powder 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:
55758-319-04
Package Description:
113 g in 1 BOTTLE
Product Code:
55758-319
Proprietary Name:
Rapidol Sodium Bicarbonate
Non-Proprietary Name:
Sodium Bicarbonate
Substance Name:
Sodium Bicarbonate
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
11-Digit NDC Billing Format:
55758031904
NDC to RxNorm Crosswalk:
  • RxCUI: 1488624 - sodium bicarbonate 2.6 GM Powder for Oral Solution
  • RxCUI: 1488624 - sodium bicarbonate 2600 MG Powder for Oral Solution
  • RxCUI: 1488624 - NaHCO3 2600 MG Powder for Oral Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Pharmadel Llc
    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(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • SODIUM BICARBONATE 2.6 g/2.6g
    • 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:
    11-23-2020
    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 55758-319-04?

    The NDC Packaged Code 55758-319-04 is assigned to a package of 113 g in 1 bottle of Rapidol Sodium Bicarbonate, a human over the counter drug labeled by Pharmadel Llc. The product's dosage form is powder and is administered via oral form.

    Is NDC 55758-319 included in the NDC Directory?

    Yes, Rapidol Sodium Bicarbonate with product code 55758-319 is active and included in the NDC Directory. The product was first marketed by Pharmadel Llc on November 23, 2020 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 11-digit format for NDC 55758-319-04?

    The 11-digit format is 55758031904. 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
    5-3-255758-319-045-4-255758-0319-04