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  5. NDC Package Code: 51672-4178-4 Iloperidone

NDC Package 51672-4178-4 Iloperidone

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
51672-4178-4
Package Description:
60 TABLET in 1 BOTTLE
Product Code:
51672-4178
Proprietary Name:
Iloperidone
Usage Information:
Iloperidone tablets are indicated for the treatment of schizophrenia in adults.When deciding among the alternative treatments available for this condition, the prescriber should consider the finding that iloperidone tablets are associated with prolongation of the QTc interval [see Warnings and Precautions (5.3)]. Prolongation of the QTc interval is associated in some other drugs with the ability to cause torsade de pointes-type arrhythmia, a potentially fatal polymorphic ventricular tachycardia which can result in sudden death. In many cases this would lead to the conclusion that other drugs should be tried first. Whether iloperidone tablets will cause torsade de pointes or increase the rate of sudden death is not yet known. Patients must be titrated to an effective dose of iloperidone tablets. Thus, control of symptoms may be delayed during the first 1 to 2 weeks of treatment compared to some other antipsychotic drugs that do not require a similar titration. Prescribers should be mindful of this delay when selecting an antipsychotic drug for the treatment of schizophrenia [see Dosage and Administration (2.1) and Clinical Studies (14)].
11-Digit NDC Billing Format:
51672417804
NDC to RxNorm Crosswalk:
Labeler Name:
-sun Pharmaceutical Industries, Inc.
Sample Package:
No
FDA Application Number:
ANDA207098
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-22-2019
End Marketing Date:
09-03-2025
Listing Expiration Date:
09-03-2025
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.

Frequently Asked Questions

What is NDC 51672-4178-4?

The NDC Packaged Code 51672-4178-4 is assigned to a package of 60 tablet in 1 bottle of Iloperidone, labeled by -sun Pharmaceutical Industries, Inc.. The product's dosage form is and is administered via form.

Is NDC 51672-4178 included in the NDC Directory?

No, Iloperidone with product code 51672-4178 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by -sun Pharmaceutical Industries, Inc. on July 22, 2019 and its listing in the NDC Directory is set to expire on September 03, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 51672-4178-4?

The 11-digit format is 51672417804. 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
5-4-151672-4178-45-4-251672-4178-04