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  5. NDC Package Code: 0404-9978-30 Sodium Chloride

NDC Package 0404-9978-30 Sodium Chloride

Injection, Solution, Concentrate Intravenous - 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:
0404-9978-30
Package Description:
1 VIAL in 1 BAG / 30 mL in 1 VIAL
Product Code:
0404-9978
Proprietary Name:
Sodium Chloride
Non-Proprietary Name:
Sodium Chloride
Substance Name:
Sodium Chloride
Usage Information:
This solution is used to supply water and salt (sodium chloride) to the body. Sodium chloride solution may also be mixed with other medications given by injection into a vein.
11-Digit NDC Billing Format:
00404997830
NDC to RxNorm Crosswalk:
  • RxCUI: 1807571 - sodium chloride 23.4 % in 30 ML Injection
  • RxCUI: 1807571 - 30 ML sodium chloride 234 MG/ML Injection
  • RxCUI: 1807571 - 30 ML NaCl 234 MG/ML Injection
  • RxCUI: 1807571 - sodium chloride 120 MEQ per 30 ML Injection
  • RxCUI: 1807571 - sodium chloride 23.4 % per 30 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Henry Schein, Inc.
    Dosage Form:
    Injection, Solution, Concentrate - A sterile preparation for parenteral use which, upon the addition of suitable solvents, yields a solution conforming in all respects to the requirements for Injections.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • SODIUM CHLORIDE 4 meq/mL
    • Sample Package:
    No
    FDA Application Number:
    ANDA212248
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-12-2022
    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 0404-9978-30?

    The NDC Packaged Code 0404-9978-30 is assigned to a package of 1 vial in 1 bag / 30 ml in 1 vial of Sodium Chloride, a human prescription drug labeled by Henry Schein, Inc.. The product's dosage form is injection, solution, concentrate and is administered via intravenous form.

    Is NDC 0404-9978 included in the NDC Directory?

    Yes, Sodium Chloride with product code 0404-9978 is active and included in the NDC Directory. The product was first marketed by Henry Schein, Inc. on January 12, 2022 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 0404-9978-30?

    The 11-digit format is 00404997830. 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 4-4-2 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
    4-4-20404-9978-305-4-200404-9978-30