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  5. NDC Package Code: 51672-2083-8 Terbinafine Hydrochloride

NDC Package 51672-2083-8 Terbinafine 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:
51672-2083-8
Package Description:
1 TUBE in 1 CARTON / 12 g in 1 TUBE
Product Code:
51672-2083
Proprietary Name:
Terbinafine Hydrochloride
Usage Information:
Adults and children 12 years and over:use the tip of the cap to break the seal and open the tubewash the affected skin with soap and water and dry completely before applyingapply once a day (morning or night) for 1 week or as directed by a doctorwash hands after each usechildren under 12 years: ask a doctor
11-Digit NDC Billing Format:
51672208308
NDC to RxNorm Crosswalk:
  • RxCUI: 992528 - terbinafine HCl 1 % Topical Cream
  • RxCUI: 992528 - terbinafine hydrochloride 10 MG/ML Topical Cream
  • RxCUI: 992528 - terbinafine hydrochloride 1 % Topical Cream
    • Labeler Name:
    Taro Pharmaceuticals U.s.a., Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-02-2007
    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 51672-2083-8?

    The NDC Packaged Code 51672-2083-8 is assigned to a package of 1 tube in 1 carton / 12 g in 1 tube of Terbinafine Hydrochloride, labeled by Taro Pharmaceuticals U.s.a., Inc.. The product's dosage form is and is administered via form.

    Is NDC 51672-2083 included in the NDC Directory?

    No, Terbinafine Hydrochloride with product code 51672-2083 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 July 02, 2007 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 11-digit format for NDC 51672-2083-8?

    The 11-digit format is 51672208308. 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
    5-4-151672-2083-85-4-251672-2083-08