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  5. NDC Package Code: 0781-1681-31 Ondansetron

NDC Package 0781-1681-31 Ondansetron

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

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
0781-1681-31
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
0781-1681
Proprietary Name:
Ondansetron
11-Digit NDC Billing Format:
00781168131
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
Labeler Name:
Sandoz Inc
Sample Package:
No
FDA Application Number:
ANDA077517
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-25-2007
End Marketing Date:
11-30-2019
Listing Expiration Date:
11-30-2019
Exclude Flag:
D
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 0781-1681-31 HCPCS crosswalk information with package details and bill units information.

NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
00781168131Q0162ONDANSETRON 1 MG, ORAL, FDA APPROVED PRESCRIPTION ANTI-EMETIC, FOR USE AS A COMPLETE THERAPEUTIC SUBSTITUTE FOR AN IV ANTI-EMETIC AT THE TIME OF CHEMOTHERAPY TREATMENT, NOT TO EXCEED A 48 HOUR DOSAGE REGIMEN1 MG30EA

* Please review the disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0781-1681-331 BLISTER PACK in 1 CARTON / 3 TABLET, FILM COATED in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0781-1681-31?

The NDC Packaged Code 0781-1681-31 is assigned to a package of 30 tablet, film coated in 1 bottle of Ondansetron, labeled by Sandoz Inc. The product's dosage form is and is administered via form.

Is NDC 0781-1681 included in the NDC Directory?

No, Ondansetron with product code 0781-1681 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sandoz Inc on June 25, 2007 and its listing in the NDC Directory is set to expire on November 30, 2019 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0781-1681-31?

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 0781-1681-31?

The 11-digit format is 00781168131. 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 4-4-2 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
4-4-20781-1681-315-4-200781-1681-31