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  5. NDC Package Code: 50090-3839-0 Ondansetron

NDC Package 50090-3839-0 Ondansetron

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
50090-3839-0
Package Description:
25 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE
Product Code:
50090-3839
Proprietary Name:
Ondansetron
Usage Information:
Ondansetron Injection is contraindicated for patients known to have hypersensitivity (e.g., anaphylaxis) to this product or any of its components. Anaphylactic reactions have been reported in patients taking ondansetron. [See Adverse Reactions (6.2).] The concomitant use of apomorphine with ondansetron is contraindicated based on reports of profound hypotension and loss of consciousness when apomorphine was administered with ondansetron.
11-Digit NDC Billing Format:
50090383900
NDC to RxNorm Crosswalk:
  • RxCUI: 1740467 - ondansetron 4 MG in 2 ML Injection
  • RxCUI: 1740467 - 2 ML ondansetron 2 MG/ML Injection
  • RxCUI: 1740467 - ondansetron 4 MG per 2 ML Injection
    • Labeler Name:
    A-s Medication Solutions
    Sample Package:
    No
    Start Marketing Date:
    12-21-2012
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 50090-3839-0?

    The NDC Packaged Code 50090-3839-0 is assigned to a package of 25 vial, single-dose in 1 carton / 2 ml in 1 vial, single-dose of Ondansetron, labeled by A-s Medication Solutions. The product's dosage form is and is administered via form.

    Is NDC 50090-3839 included in the NDC Directory?

    No, Ondansetron with product code 50090-3839 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by A-s Medication Solutions on December 21, 2012 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50090-3839-0?

    The 11-digit format is 50090383900. 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 5-4-1 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
    5-4-150090-3839-05-4-250090-3839-00