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  5. NDC Package Code: 51141-0070-5 Triple Antibiotic Ointment

NDC Package 51141-0070-5 Triple Antibiotic Ointment

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:
51141-0070-5
Package Description:
1 TUBE in 1 BOX / 14 g in 1 TUBE
Product Code:
51141-0070
Proprietary Name:
Triple Antibiotic Ointment
Usage Information:
Adults and children 2 years of age or older:clean the affected areaapply a small amount of this product (an amount equal tot the surface area of the tip of a finer) on the area 1 to 3 times dailymay be covered with a sterile bandagechildren under 2 years of age:  ask a doctor
11-Digit NDC Billing Format:
51141007005
NDC to RxNorm Crosswalk:
  • RxCUI: 204602 - bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical Ointment
  • RxCUI: 204602 - bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment
  • RxCUI: 204602 - bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical Ointment
    • Labeler Name:
    Neopharm Co., Ltd
    Sample Package:
    No
    Start Marketing Date:
    09-01-2010
    Listing Expiration Date:
    12-31-2017
    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
    51141-0070-11 TUBE in 1 BOX / 28 g in 1 TUBE
    51141-0070-31 TUBE in 1 BOX / 9.4 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51141-0070-5?

    The NDC Packaged Code 51141-0070-5 is assigned to a package of 1 tube in 1 box / 14 g in 1 tube of Triple Antibiotic Ointment, labeled by Neopharm Co., Ltd. The product's dosage form is and is administered via form.

    Is NDC 51141-0070 included in the NDC Directory?

    No, Triple Antibiotic Ointment with product code 51141-0070 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Neopharm Co., Ltd on September 01, 2010 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51141-0070-5?

    The 11-digit format is 51141007005. 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
    5-4-151141-0070-55-4-251141-0070-05