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  5. NDC Package Code: 68788-9368-3 Ondansetron Hydrochloride

NDC Package 68788-9368-3 Ondansetron Hydrochloride

Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Other Packages
    4. 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:
68788-9368-3
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
68788-9368
Proprietary Name:
Ondansetron Hydrochloride
Non-Proprietary Name:
Ondansetron Hydrochloride
Substance Name:
Ondansetron Hydrochloride
Usage Information:
Ondansetron tablets are indicated for the prevention of nausea and vomiting associated with:•highly emetogenic cancer chemotherapy, including cisplatin greater than or equal to 50 mg/m2.•initial and repeat courses of moderately emetogenic cancer chemotherapy.•radiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomen.Ondansetron tablets are also indicated for the prevention of postoperative nausea and/or vomiting.
11-Digit NDC Billing Format:
68788936803
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 198052 - ondansetron HCl 4 MG Oral Tablet
  • RxCUI: 198052 - ondansetron 4 MG Oral Tablet
  • RxCUI: 198052 - ondansetron 4 MG (as ondansetron HCl dihydrate 5 MG) Oral Tablet
  • RxCUI: 312086 - ondansetron HCl 8 MG Oral Tablet
  • RxCUI: 312086 - ondansetron 8 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Preferred Pharmaceuticals, Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ONDANSETRON HYDROCHLORIDE 4 mg/1
    • 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:
    ANDA078539
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-12-2012
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 68788-9368-3 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    68788936803Q0162Ondansetron oral1 MG301120120

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    68788-9368-110 TABLET, FILM COATED in 1 BOTTLE
    68788-9368-212 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68788-9368-3?

    The NDC Packaged Code 68788-9368-3 is assigned to a package of 30 tablet, film coated in 1 bottle of Ondansetron Hydrochloride, a human prescription drug labeled by Preferred Pharmaceuticals, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package.

    Is NDC 68788-9368 included in the NDC Directory?

    Yes, Ondansetron Hydrochloride with product code 68788-9368 is active and included in the NDC Directory. The product was first marketed by Preferred Pharmaceuticals, Inc. on June 12, 2012 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 NDC billing unit for package 68788-9368-3?

    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 30.

    What is the 11-digit format for NDC 68788-9368-3?

    The 11-digit format is 68788936803. 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
    5-4-168788-9368-35-4-268788-9368-03