NDC Package 0338-0126-12 Myxredlin

Insulin Human 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:
0338-0126-12
Package Description:
12 CONTAINER in 1 CARTON / 100 mL in 1 CONTAINER
Product Code:
Proprietary Name:
Myxredlin
Non-Proprietary Name:
Insulin Human
Substance Name:
Insulin Human
Usage Information:
MYXREDLIN is indicated to improve glycemic control in adults and pediatric patients with diabetes mellitus.
11-Digit NDC Billing Format:
00338012612
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2179744 - regular insulin, human 100 UNT in 100 ML Injection
  • RxCUI: 2179744 - 100 ML insulin, regular, human 1 UNT/ML Injection
  • RxCUI: 2179744 - regular insulin, human 100 UNT per 100 ML Injection
  • RxCUI: 2179749 - MYXREDLIN 100 UNT in 100 ML Injection
  • RxCUI: 2179749 - 100 ML insulin, regular, human 1 UNT/ML Injection [Myxredlin]
  • 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:
    BLA208157
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    07-12-2019
    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 0338-0126-12?

    The NDC Packaged Code 0338-0126-12 is assigned to a package of 12 container in 1 carton / 100 ml in 1 container of Myxredlin, 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 0338-0126 included in the NDC Directory?

    Yes, Myxredlin with product code 0338-0126 is active and included in the NDC Directory. The product was first marketed by Baxter Healthcare Corporation on July 12, 2019 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 0338-0126-12?

    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 0338-0126-12?

    The 11-digit format is 00338012612. 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
    4-4-20338-0126-125-4-200338-0126-12