NDC Package 50436-1880-1 Ondansetron Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

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:

50436-1880-1

Package Description:

30 TABLET, FILM COATED in 1 BOTTLE

Product Code:

50436-1880

Proprietary 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:

50436188001

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

Labeler Name:

Unit Dose Services

Sample Package:

Start Marketing Date:

07-31-2007

Listing Expiration Date:

12-31-2022

Exclude Flag:

Code Structure:

50436 - Unit Dose Services
- 50436-1880 - Ondansetron Hydrochloride
  - 50436-1880-1 - 30 TABLET, FILM COATED in 1 BOTTLE

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 50436-1880-1?

The NDC Packaged Code 50436-1880-1 is assigned to a package of 30 tablet, film coated in 1 bottle of Ondansetron Hydrochloride, labeled by Unit Dose Services. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package.

Is NDC 50436-1880 included in the NDC Directory?

No, Ondansetron Hydrochloride with product code 50436-1880 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Unit Dose Services on July 31, 2007 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 50436-1880-1?

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 50436-1880-1?

The 11-digit format is 50436188001. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	50436-1880-1	5-4-2	50436-1880-01

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