NDC Package 10544-575-06 Ondansetron Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

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:
10544-575-06
Package Description:
6 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Ondansetron Hydrochloride
Usage Information:
Prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy, including cisplatin ≥50 mg/m 2. 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 tablets, USP are recommended even where the incidence of postoperative nausea and/or vomiting is low.
11-Digit NDC Billing Format:
10544057506
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
6 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 312086 - ondansetron HCl 8 MG Oral Tablet
  • RxCUI: 312086 - ondansetron 8 MG Oral Tablet
  • RxCUI: 312086 - ondansetron 8 MG (as ondansetron HCl dihydrate 10 MG) Oral Tablet
  • Labeler Name:
    Blenheim Pharmacal, Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-17-2013
    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 10544-575-06?

    The NDC Packaged Code 10544-575-06 is assigned to a package of 6 tablet, film coated in 1 bottle of Ondansetron Hydrochloride, labeled by Blenheim Pharmacal, Inc.. The product's dosage form is and is administered via form.

    Is NDC 10544-575 included in the NDC Directory?

    No, Ondansetron Hydrochloride with product code 10544-575 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Blenheim Pharmacal, Inc. on December 17, 2013 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 NDC billing unit for package 10544-575-06?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 6.

    What is the 11-digit format for NDC 10544-575-06?

    The 11-digit format is 10544057506. 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
    5-3-210544-575-065-4-210544-0575-06