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  5. NDC Package Code: 0409-7101-02 Sodium Chloride

NDC Package 0409-7101-02 Sodium Chloride

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

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Other Packages
    4. 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:
0409-7101-02
Package Description:
24 POUCH in 1 CASE / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-7101-04)
Product Code:
0409-7101
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:
00409710102
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1807547 - sodium chloride 4.5 MG/ML Injection
  • RxCUI: 1807547 - NaCl 4.5 MG/ML Injection
  • RxCUI: 1807631 - sodium chloride 0.9 % in 50 ML Injection
  • RxCUI: 1807631 - 50 ML sodium chloride 9 MG/ML Injection
  • RxCUI: 1807631 - 50 ML NaCl 9 MG/ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hospira, Inc.
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • SODIUM CHLORIDE 900 mg/100mL
    • Pharmacologic Class(es):
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA019465
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-30-2005
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 0409-7101-02 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    00409710102J7030Normal saline solution infus1000 CC250240.256
    00409710102J7040Normal saline solution infus500 ML250240.512
    00409710102J7050Normal saline solution infus250 CC25024124

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0409-7101-6610 POUCH in 1 CASE / 5 BAG in 1 POUCH / 50 mL in 1 BAG (0409-7101-68)
    0409-7101-6710 POUCH in 1 CASE / 5 BAG in 1 POUCH / 100 mL in 1 BAG (0409-7101-69)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0409-7101-02?

    The NDC Packaged Code 0409-7101-02 is assigned to a package of 24 pouch in 1 case / 1 bag in 1 pouch / 250 ml in 1 bag (0409-7101-04) of Sodium Chloride, a human prescription drug labeled by Hospira, Inc.. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 0409-7101 included in the NDC Directory?

    Yes, Sodium Chloride with product code 0409-7101 is active and included in the NDC Directory. The product was first marketed by Hospira, Inc. on June 30, 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 0409-7101-02?

    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 0409-7101-02?

    The 11-digit format is 00409710102. 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
    4-4-20409-7101-025-4-200409-7101-02