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  5. NDC Package Code: 51141-6010-1 Atopalm Maximum Strength Anti-itch

NDC Package 51141-6010-1 Atopalm Maximum Strength Anti-itch

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:
51141-6010-1
Package Description:
1 TUBE in 1 CARTON / 28.3 g in 1 TUBE
Product Code:
51141-6010
Proprietary Name:
Atopalm Maximum Strength Anti-itch
Usage Information:
Adults and children 2 years of age and older  - apply to affected area not more than 3 to 4 times daily Children under 2 years of age - Do not use. Consult a doctor. For external anal itching - adults, when practical, cleanse the affected area with mild soap, and warm water, and rinse thoroughly, or by patting or blotting with toilet tissue or a soft cloth before application of this product. - children under 12 years of age with external anal itching, consult a doctor.
11-Digit NDC Billing Format:
51141601001
NDC to RxNorm Crosswalk:
  • RxCUI: 203105 - hydrocortisone 1 % Topical Ointment
  • RxCUI: 203105 - hydrocortisone 0.01 MG/MG Topical Ointment
    • Labeler Name:
    Neopharm Co., Ltd.
    Sample Package:
    No
    Start Marketing Date:
    11-04-2011
    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.

    Frequently Asked Questions

    What is NDC 51141-6010-1?

    The NDC Packaged Code 51141-6010-1 is assigned to a package of 1 tube in 1 carton / 28.3 g in 1 tube of Atopalm Maximum Strength Anti-itch, labeled by Neopharm Co., Ltd.. The product's dosage form is and is administered via form.

    Is NDC 51141-6010 included in the NDC Directory?

    No, Atopalm Maximum Strength Anti-itch with product code 51141-6010 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 November 04, 2011 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 51141-6010-1?

    The 11-digit format is 51141601001. 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
    5-4-151141-6010-15-4-251141-6010-01