NDC Package 68084-950-01 Fluphenazine Hydrochloride

Tablet, Film Coated 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:
68084-950-01
Package Description:
100 BLISTER PACK in 1 BOX, UNIT-DOSE / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-950-11)
Product Code:
Proprietary Name:
Fluphenazine Hydrochloride
Non-Proprietary Name:
Fluphenazine Hydrochloride
Substance 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:
68084095001
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 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
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    American Health Packaging
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA089743
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-01-2015
    End Marketing Date:
    04-30-2025
    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 68084-950-01?

    The NDC Packaged Code 68084-950-01 is assigned to a package of 100 blister pack in 1 box, unit-dose / 1 tablet, film coated in 1 blister pack (68084-950-11) of Fluphenazine Hydrochloride, a human prescription drug labeled by American Health Packaging. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 68084-950 included in the NDC Directory?

    Yes, Fluphenazine Hydrochloride with product code 68084-950 is active and included in the NDC Directory. The product was first marketed by American Health Packaging on October 01, 2015.

    What is the NDC billing unit for package 68084-950-01?

    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 100.

    What is the 11-digit format for NDC 68084-950-01?

    The 11-digit format is 68084095001. 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
    5-3-268084-950-015-4-268084-0950-01