NDC Package 0409-6660-75 Sodium Chloride

Injection, Solution, Concentrate Intravenous - View Billable Units, 11-Digit Format, RxNorm

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:
0409-6660-75
Package Description:
25 VIAL in 1 TRAY / 40 mL in 1 VIAL (0409-6660-01)
Product Code:
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:
00409666075
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1807578 - sodium chloride 14.6 % in 20 ML Injection
  • RxCUI: 1807578 - 20 ML sodium chloride 146 MG/ML Injection
  • RxCUI: 1807578 - 20 ML NaCl 146 MG/ML Injection
  • RxCUI: 1807578 - sodium chloride 14.6 % per 20 ML Injection
  • RxCUI: 1807580 - sodium chloride 14.6 % in 40 ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hospira, 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):
    Sample Package:
    No
    FDA Application Number:
    NDA018897
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    07-29-2005
    Listing Expiration Date:
    12-31-2025
    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 0409-6660-75?

    The NDC Packaged Code 0409-6660-75 is assigned to a package of 25 vial in 1 tray / 40 ml in 1 vial (0409-6660-01) of Sodium Chloride, a human prescription drug labeled by Hospira, Inc.. The product's dosage form is injection, solution, concentrate and is administered via intravenous form.

    Is NDC 0409-6660 included in the NDC Directory?

    Yes, Sodium Chloride with product code 0409-6660 is active and included in the NDC Directory. The product was first marketed by Hospira, Inc. on July 29, 2005 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0409-6660-75?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0409-6660-75?

    The 11-digit format is 00409666075. 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
    4-4-20409-6660-755-4-200409-6660-75