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  5. NDC Package Code: 68788-7449-1 Fexofenadine Hcl

NDC Package 68788-7449-1 Fexofenadine Hcl

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
68788-7449-1
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
68788-7449
Proprietary Name:
Fexofenadine Hcl
Non-Proprietary Name:
Fexofenadine Hcl
Substance Name:
Fexofenadine Hydrochloride
Usage Information:
Fexofenadine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction.
11-Digit NDC Billing Format:
68788744901
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: 997420 - fexofenadine HCl 180 MG 24 HR Oral Tablet
  • RxCUI: 997420 - fexofenadine hydrochloride 180 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Preferred Pharmaceuticals, 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):
  • FEXOFENADINE HYDROCHLORIDE 180 mg/1
    • Pharmacologic Class(es):
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA204097
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-19-2016
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    68788-7449-330 TABLET in 1 BOTTLE
    68788-7449-660 TABLET in 1 BOTTLE
    68788-7449-990 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68788-7449-1?

    The NDC Packaged Code 68788-7449-1 is assigned to a package of 100 tablet in 1 bottle of Fexofenadine Hcl, a human over the counter drug labeled by Preferred Pharmaceuticals, Inc.. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 100 billable units per package.

    Is NDC 68788-7449 included in the NDC Directory?

    Yes, Fexofenadine Hcl with product code 68788-7449 is active and included in the NDC Directory. The product was first marketed by Preferred Pharmaceuticals, Inc. on August 19, 2016 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 NDC billing unit for package 68788-7449-1?

    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 100.

    What is the 11-digit format for NDC 68788-7449-1?

    The 11-digit format is 68788744901. 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
    5-4-168788-7449-15-4-268788-7449-01