NDC Package 55648-726-01 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:
55648-726-01
Package Description:
5 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE
Product Code:
Proprietary Name:
Ondansetron Hydrochloride
Usage Information:
Prevention of nausea and vomiting associated with initial and repeat courses of emetogenic cancer chemotherapy, including high-dose cisplatin. Efficacy of the 32-mg single dose beyond 24 hours in these patients has not been established. 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 injection is recommended even where the incidence of postoperative nausea and/or vomiting is low. For patients who do not receive prophylactic ondansetron injection and experience nausea and/or vomiting postoperatively, ondansetron injection may be given to prevent further episodes (see CLINICAL TRIALS).
11-Digit NDC Billing Format:
55648072601
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
  • RxCUI: 283504 - ondansetron 2 MG/ML Injectable Solution
  • RxCUI: 283504 - ondansetron (as ondansetron HCl ) 2 MG/ML Injectable Solution
  • Labeler Name:
    Wockhardt Limited
    Sample Package:
    No
    FDA Application Number:
    ANDA077716
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-27-2006
    Listing Expiration Date:
    12-31-2018
    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 55648-726-01?

    The NDC Packaged Code 55648-726-01 is assigned to a package of 5 vial, single-dose in 1 carton / 2 ml in 1 vial, single-dose of Ondansetron Hydrochloride, labeled by Wockhardt Limited. The product's dosage form is and is administered via form.

    Is NDC 55648-726 included in the NDC Directory?

    No, Ondansetron Hydrochloride with product code 55648-726 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Wockhardt Limited on December 27, 2006 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55648-726-01?

    The 11-digit format is 55648072601. 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
    5-3-255648-726-015-4-255648-0726-01