NDC Package 0338-0431-03 Heparin Sodium In Sodium Chloride

Heparin Sodium Injection, Solution 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:
0338-0431-03
Package Description:
18 BAG in 1 CARTON / 500 mL in 1 BAG
Product Code:
Proprietary Name:
Heparin Sodium In Sodium Chloride
Non-Proprietary Name:
Heparin Sodium
Substance Name:
Heparin Sodium
Usage Information:
Heparin Sodium and 0.9% Sodium Chloride Injection at a concentration of 2 units/mL is indicated as an aid in the maintenance of catheter patency.
11-Digit NDC Billing Format:
00338043103
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1658690 - heparin sodium, porcine 2000 UNT in 1000 ML Injection
  • RxCUI: 1658690 - 1000 ML heparin sodium, porcine 2 UNT/ML Injection
  • RxCUI: 1658690 - heparin sodium, porcine 2000 UNT per 1000 ML Injection
  • RxCUI: 1658692 - heparin sodium, porcine 1000 UNT in 500 ML Injection
  • RxCUI: 1658692 - 500 ML heparin sodium, porcine 2 UNT/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Baxter Healthcare Corporation
    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):
    Sample Package:
    No
    FDA Application Number:
    NDA018609
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    04-28-1982
    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 0338-0431-03?

    The NDC Packaged Code 0338-0431-03 is assigned to a package of 18 bag in 1 carton / 500 ml in 1 bag of Heparin Sodium In Sodium Chloride, a human prescription drug labeled by Baxter Healthcare Corporation. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 0338-0431 included in the NDC Directory?

    Yes, Heparin Sodium In Sodium Chloride with product code 0338-0431 is active and included in the NDC Directory. The product was first marketed by Baxter Healthcare Corporation on April 28, 1982 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 NDC billing unit for package 0338-0431-03?

    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 0338-0431-03?

    The 11-digit format is 00338043103. 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
    4-4-20338-0431-035-4-200338-0431-03