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  5. NDC Package Code: 54868-2338-4 Biaxin

NDC Package 54868-2338-4 Biaxin

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

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

Package Information

This product is EXCLUDED from the official NDC directory .

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:
54868-2338-4
Package Description:
120 TABLET, FILM COATED in 1 BOTTLE
Product Code:
54868-2338
Proprietary Name:
Biaxin
Usage Information:
BIAXIN Filmtab (clarithromycin tablets, USP) and BIAXIN Granules (clarithromycin for oral suspension, USP) are indicated for the treatment of mild to moderate infections caused by susceptible strains of the designated microorganisms in the conditions as listed below:
11-Digit NDC Billing Format:
54868233804
NDC to RxNorm Crosswalk:
  • RxCUI: 197516 - clarithromycin 250 MG Oral Tablet
  • RxCUI: 197517 - clarithromycin 500 MG Oral Tablet
  • RxCUI: 205857 - clarithromycin 25 MG/ML Oral Suspension [Biaxin]
  • RxCUI: 205857 - Biaxin 125 MG per 5 ML Granules for Oral Suspension
  • RxCUI: 205857 - Biaxin 25 MG/ML Oral Suspension
    • Labeler Name:
    Physicians Total Care, Inc.
    Sample Package:
    No
    FDA Application Number:
    NDA050662
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-23-1993
    End Marketing Date:
    06-30-2011
    Listing Expiration Date:
    06-30-2011
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    54868-2338-05 TABLET, FILM COATED in 1 BOTTLE
    54868-2338-120 TABLET, FILM COATED in 1 BOTTLE
    54868-2338-214 TABLET, FILM COATED in 1 BOTTLE
    54868-2338-360 TABLET, FILM COATED in 1 BOTTLE
    54868-2338-530 TABLET, FILM COATED in 1 BLISTER PACK
    54868-2338-610 TABLET, FILM COATED in 1 BOTTLE
    54868-2338-715 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 54868-2338-4?

    The NDC Packaged Code 54868-2338-4 is assigned to a package of 120 tablet, film coated in 1 bottle of Biaxin, labeled by Physicians Total Care, Inc.. The product's dosage form is and is administered via form.

    Is NDC 54868-2338 included in the NDC Directory?

    The product was first marketed by Physicians Total Care, Inc. on June 23, 1993 and its listing in the NDC Directory is set to expire on June 30, 2011 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 54868-2338-4?

    The 11-digit format is 54868233804. 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
    5-4-154868-2338-45-4-254868-2338-04