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  5. NDC Package Code: 71872-7140-1 Ondansetron

NDC Package 71872-7140-1 Ondansetron

Injection Intramuscular; Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
71872-7140-1
Package Description:
1 VIAL in 1 BAG / 2 mL in 1 VIAL
Product Code:
71872-7140
Proprietary Name:
Ondansetron
Non-Proprietary Name:
Ondansetron
Substance Name:
Ondansetron Hydrochloride
Usage Information:
This medication is used alone or with other medications to prevent nausea and vomiting caused by cancer drug treatment (chemotherapy) and radiation therapy. It is also used to prevent and treat nausea and vomiting after surgery. Ondansetron works by blocking one of the body's natural substances (serotonin) that causes vomiting.
11-Digit NDC Billing Format:
71872714001
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
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Medical Purchasing Solutions, Llc
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • ONDANSETRON HYDROCHLORIDE 2 mg/mL
    • Pharmacologic Class(es):
  • Serotonin 3 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Serotonin-3 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA077541
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-26-2006
    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 71872-7140-1?

    The NDC Packaged Code 71872-7140-1 is assigned to a package of 1 vial in 1 bag / 2 ml in 1 vial of Ondansetron, a human prescription drug labeled by Medical Purchasing Solutions, Llc. The product's dosage form is injection and is administered via intramuscular; intravenous form.

    Is NDC 71872-7140 included in the NDC Directory?

    Yes, Ondansetron with product code 71872-7140 is active and included in the NDC Directory. The product was first marketed by Medical Purchasing Solutions, Llc on December 26, 2006 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 11-digit format for NDC 71872-7140-1?

    The 11-digit format is 71872714001. 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
    5-4-171872-7140-15-4-271872-7140-01