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  5. NDC Package Code: 68788-823-01 Ondansetron Hydrochloride

NDC Package 68788-823-01 Ondansetron Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
68788-823-01
Package Description:
10 BLISTER PACK in 1 DOSE PACK / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
68788-823
Proprietary Name:
Ondansetron Hydrochloride
Usage Information:
Carvedilol is contraindicated in the following conditions:•Bronchial asthma or related bronchospastic conditions. Deaths from status asthmaticus have been reported following single doses of carvedilol. •Second- or third-degree AV block. •Sick sinus syndrome. •Severe bradycardia (unless a permanent pacemaker is in place). •Patients with cardiogenic shock or who have decompensated heart failure requiring the use of intravenous inotropic therapy. Such patients should first be weaned from intravenous therapy before initiating carvedilol. •Patients with severe hepatic impairment. •Patients with a history of a serious hypersensitivity reaction (e.g., Stevens-Johnson syndrome, anaphylactic reaction, angioedema) to any component of this medication or other medications containing carvedilol.
11-Digit NDC Billing Format:
68788082301
NDC to RxNorm Crosswalk:
RxCUI: 200033 - carvedilol 25 MG Oral Tablet
Labeler Name:
Preferred Pharmaceuticals, Inc
Sample Package:
No
FDA Application Number:
ANDA077050
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-25-2007
End Marketing Date:
04-28-2011
Listing Expiration Date:
04-28-2011
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
68788-823-0330 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68788-823-01?

The NDC Packaged Code 68788-823-01 is assigned to a package of 10 blister pack in 1 dose pack / 10 tablet, film coated in 1 blister pack of Ondansetron Hydrochloride, labeled by Preferred Pharmaceuticals, Inc. The product's dosage form is and is administered via form.

Is NDC 68788-823 included in the NDC Directory?

No, Ondansetron Hydrochloride with product code 68788-823 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Preferred Pharmaceuticals, Inc on June 25, 2007 and its listing in the NDC Directory is set to expire on April 28, 2011 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 68788-823-01?

The 11-digit format is 68788082301. 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
5-3-268788-823-015-4-268788-0823-01