NDC Package 44523-607-01 Sodium Sulfacetamide And Sulfur

Sulfacetamide Sodium,Sulfur Lotion Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
44523-607-01
Package Description:
30 g in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Sodium Sulfacetamide And Sulfur
Non-Proprietary Name:
Sulfacetamide Sodium, Sulfur
Substance Name:
Sulfacetamide Sodium; Sulfur
Usage Information:
This product is indicated for use in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.
11-Digit NDC Billing Format:
44523060701
NDC to RxNorm Crosswalk:
  • RxCUI: 1005856 - sulfacetamide sodium 10 % / sulfur 5 % Topical Lotion
  • RxCUI: 1005856 - sulfacetamide sodium 100 MG/ML / sulfur 50 MG/ML Topical Lotion
  • RxCUI: 1005856 - sulfacetamide sodium 10 % / sulfur 5 % Topical Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Biocomp Pharma, Inc.
    Dosage Form:
    Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    06-04-2011
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    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
    44523-607-0260 g in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 44523-607-01?

    The NDC Packaged Code 44523-607-01 is assigned to a package of 30 g in 1 bottle, plastic of Sodium Sulfacetamide And Sulfur, a human prescription drug labeled by Biocomp Pharma, Inc.. The product's dosage form is lotion and is administered via topical form.

    Is NDC 44523-607 included in the NDC Directory?

    Yes, Sodium Sulfacetamide And Sulfur with product code 44523-607 is active and included in the NDC Directory. The product was first marketed by Biocomp Pharma, Inc. on June 04, 2011 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 44523-607-01?

    The 11-digit format is 44523060701. 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
    5-3-244523-607-015-4-244523-0607-01