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  5. NDC Package Code: 51672-4233-1 Fluphenazine Hydrochloride

NDC Package 51672-4233-1 Fluphenazine Hydrochloride

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 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:
51672-4233-1
Package Description:
1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE
Product Code:
51672-4233
Proprietary Name:
Fluphenazine Hydrochloride
Usage Information:
Fluphenazine hydrochloride tablets are indicated in the management of manifestations of psychotic disorders.Fluphenazine hydrochloride has not been shown effective in the management of behavioral complications in patients with mental retardation.
11-Digit NDC Billing Format:
51672423301
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 859841 - fluPHENAZine HCl 10 MG Oral Tablet
  • RxCUI: 859841 - fluphenazine hydrochloride 10 MG Oral Tablet
  • RxCUI: 860918 - fluPHENAZine HCl 5 MG Oral Tablet
  • RxCUI: 860918 - fluphenazine hydrochloride 5 MG Oral Tablet
  • RxCUI: 865117 - fluPHENAZine HCl 1 MG Oral Tablet
    • Labeler Name:
    Taro Pharmaceuticals U.s.a. Inc.
    Sample Package:
    No
    Start Marketing Date:
    04-14-2022
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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 51672-4233-1?

    The NDC Packaged Code 51672-4233-1 is assigned to a package of 1 bottle in 1 carton / 100 tablet, film coated in 1 bottle of Fluphenazine Hydrochloride, labeled by Taro Pharmaceuticals U.s.a. Inc.. The product's dosage form is and is administered via form.

    Is NDC 51672-4233 included in the NDC Directory?

    No, Fluphenazine Hydrochloride with product code 51672-4233 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Taro Pharmaceuticals U.s.a. Inc. on April 14, 2022 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 51672-4233-1?

    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 1.

    What is the 11-digit format for NDC 51672-4233-1?

    The 11-digit format is 51672423301. 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
    5-4-151672-4233-15-4-251672-4233-01