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  5. NDC Package Code: 50509-100-04 Sodium Bicarbonate

NDC Package 50509-100-04 Sodium Bicarbonate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
50509-100-04
Package Description:
4 CARTRIDGE in 1 CARTON / 1.7 mL in 1 CARTRIDGE (50509-100-03)
Product Code:
50509-100
Proprietary Name:
Sodium Bicarbonate
Usage Information:
Sodium Bicarbonate Inj., 8.4% USP Neutralizing Additive Solution is indicated to hasten onset of analgesia and reduce injection pain, by adjusting commercial preparations of Lidocaine w/ Epinephrine anesthetic solution to a more physiologic pH.
11-Digit NDC Billing Format:
50509010004
NDC to RxNorm Crosswalk:
  • RxCUI: 1868482 - sodium bicarbonate 8.4 % (1.7 MEQ) in 1.7 ML Cartridge
  • RxCUI: 1868482 - 1.7 ML sodium bicarbonate 84 MG/ML Cartridge
  • RxCUI: 1868482 - 1.7 ML NaHCO3 84 MG/ML Cartridge
  • RxCUI: 1868482 - sodium bicarbonate 8.4 % (1.7 MEQ) per 1.7 ML Cartridge
  • RxCUI: 1868485 - sodium bicarbonate 8.4 % (2.7 MEQ) in 2.7 ML Cartridge
    • Labeler Name:
    Onpharma, Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-22-2010
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50509-100-024 CARTRIDGE in 1 CARTON / 2.7 mL in 1 CARTRIDGE (50509-100-01)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50509-100-04?

    The NDC Packaged Code 50509-100-04 is assigned to a package of 4 cartridge in 1 carton / 1.7 ml in 1 cartridge (50509-100-03) of Sodium Bicarbonate, labeled by Onpharma, Inc.. The product's dosage form is and is administered via form.

    Is NDC 50509-100 included in the NDC Directory?

    No, Sodium Bicarbonate with product code 50509-100 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Onpharma, Inc. on July 22, 2010 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50509-100-04?

    The 11-digit format is 50509010004. 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
    5-3-250509-100-045-4-250509-0100-04