NDC Package 51672-4184-4 Iloperidone

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

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:
51672-4184-4
Package Description:
60 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Iloperidone
Non-Proprietary Name:
Iloperidone
Substance Name:
Iloperidone
Usage Information:
This medication is used to treat certain mental/mood disorders (such as schizophrenia). Iloperidone helps you to think more clearly, feel less nervous, and take part in everyday life. It may also help to decrease hallucinations (hearing/seeing things that are not there). Iloperidone is a psychiatric medication that belongs to the class of drugs called atypical antipsychotics. It works by helping to restore the balance of certain natural substances in the brain.
11-Digit NDC Billing Format:
51672418404
NDC to RxNorm Crosswalk:
  • RxCUI: 848722 - iloperidone 1 MG Oral Tablet
  • RxCUI: 848728 - iloperidone 10 MG Oral Tablet
  • RxCUI: 848732 - iloperidone 12 MG Oral Tablet
  • RxCUI: 848736 - iloperidone 2 MG Oral Tablet
  • RxCUI: 848740 - iloperidone 4 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Taro Pharmaceuticals U.s.a., Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    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
    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.

    Frequently Asked Questions

    What is NDC 51672-4184-4?

    The NDC Packaged Code 51672-4184-4 is assigned to a package of 60 tablet in 1 bottle of Iloperidone, a human prescription drug labeled by Taro Pharmaceuticals U.s.a., Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 51672-4184 included in the NDC Directory?

    Yes, Iloperidone with product code 51672-4184 is active and included in the NDC Directory. The product was first marketed by Taro Pharmaceuticals U.s.a., Inc. on July 22, 2019 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 11-digit format for NDC 51672-4184-4?

    The 11-digit format is 51672418404. 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
    5-4-151672-4184-45-4-251672-4184-04