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  5. NDC Package Code: 16590-545-30 Ondansetron

NDC Package 16590-545-30 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:
16590-545-30
Package Description:
30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE
Product Code:
16590-545
Proprietary Name:
Ondansetron
Usage Information:
INDICATIONS AND USAGEPrevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy, including cisplatin ≥50 mg/m2. Prevention of nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy. Prevention of nausea and vomiting associated with radiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomen. Prevention of postoperative nausea and/or vomiting. As with other antiemetics, routine prophylaxis is not recommended for patients in whom there is little expectation that nausea and/or vomiting will occur postoperatively. In patients where nausea and/or vomiting must be avoided postoperatively, ondansetron hydrochloride tablets and ondansetron orally disintegrating tablets are recommended even where the incidence of postoperative nausea and/or vomiting is low.
11-Digit NDC Billing Format:
16590054530
NDC to RxNorm Crosswalk:
  • RxCUI: 104894 - ondansetron 4 MG Disintegrating Oral Tablet
  • RxCUI: 104894 - ondansetron (as ondansetron HCl) 4 MG Disintegrating Oral Tablet
    • Labeler Name:
    Stat Rx Usa
    Sample Package:
    No
    Start Marketing Date:
    10-27-2009
    Listing Expiration Date:
    12-31-2017
    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 16590-545-30?

    The NDC Packaged Code 16590-545-30 is assigned to a package of 30 tablet, orally disintegrating in 1 bottle of Ondansetron, labeled by Stat Rx Usa. The product's dosage form is and is administered via form.

    Is NDC 16590-545 included in the NDC Directory?

    No, Ondansetron with product code 16590-545 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Stat Rx Usa on October 27, 2009 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 16590-545-30?

    The 11-digit format is 16590054530. 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 5-3-2 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
    5-3-216590-545-305-4-216590-0545-30