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  5. NDC Package Code: 55648-743-01 Terbinafine Hydrochloride

NDC Package 55648-743-01 Terbinafine Hydrochloride

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 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:
55648-743-01
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
55648-743
Proprietary Name:
Terbinafine Hydrochloride
Usage Information:
Terbinafine hydrochloride tablets are indicated for the treatment of onychomycosis of the toenail or fingernail due to dermatophytes (tinea unguium) (see DOSAGE AND ADMINISTRATION and CLINICAL STUDIES).Prior to initiating treatment, appropriate nail specimens for laboratory testing (KOH preparation, fungal culture, or nail biopsy) should be obtained to confirm the diagnosis of onychomycosis.
11-Digit NDC Billing Format:
55648074301
NDC to RxNorm Crosswalk:
  • RxCUI: 313222 - terbinafine HCl 250 MG Oral Tablet
  • RxCUI: 313222 - terbinafine 250 MG Oral Tablet
  • RxCUI: 313222 - terbinafine (as terbinafine HCl) 250 MG Oral Tablet
    • Labeler Name:
    Wockhardt Limited
    Sample Package:
    No
    Start Marketing Date:
    07-02-2007
    Listing Expiration Date:
    12-31-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    55648-743-021000 TABLET in 1 BOTTLE
    55648-743-03100 TABLET in 1 BOTTLE
    55648-743-051 BLISTER PACK in 1 CARTON / 30 TABLET in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55648-743-01?

    The NDC Packaged Code 55648-743-01 is assigned to a package of 30 tablet in 1 bottle of Terbinafine Hydrochloride, labeled by Wockhardt Limited. The product's dosage form is and is administered via form.

    Is NDC 55648-743 included in the NDC Directory?

    No, Terbinafine Hydrochloride with product code 55648-743 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Wockhardt Limited on July 02, 2007 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55648-743-01?

    The 11-digit format is 55648074301. 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
    5-3-255648-743-015-4-255648-0743-01