NDC Package 57883-404-10 Plexion

Sulfacetamide Sodium,Sulfur Cloth 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:
57883-404-10
Package Description:
10 PACKET in 1 CARTON / 4 g in 1 PACKET (57883-404-01)
Product Code:
Proprietary Name:
Plexion
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:
57883040410
NDC to RxNorm Crosswalk:
  • RxCUI: 1494170 - sulfacetamide sodium 9.8 % / sulfur 4.8 % Medicated Pad
  • RxCUI: 1494170 - sulfacetamide sodium 98 MG/ML / sulfur 48 MG/ML Medicated Pad
  • RxCUI: 1494170 - sulfacetamide sodium 9.8 % / sulfur 4.8 % Cleansing Cloth
  • RxCUI: 1494827 - Plexion 9.8 % / 4.8 % Medicated Pad
  • RxCUI: 1494827 - sulfacetamide sodium 98 MG/ML / sulfur 48 MG/ML Medicated Pad [Plexion]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Brava Pharmaceuticals, Llc
    Dosage Form:
    Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.
    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:
    Yes
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    09-01-2005
    Listing Expiration Date:
    12-31-2024
    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
    57883-404-6060 PACKET in 1 CARTON / 4 g in 1 PACKET (57883-404-01)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 57883-404-10?

    The NDC Packaged Code 57883-404-10 is assigned to a package of 10 packet in 1 carton / 4 g in 1 packet (57883-404-01) of Plexion, a human prescription drug labeled by Brava Pharmaceuticals, Llc. The product's dosage form is cloth and is administered via topical form.

    Is NDC 57883-404 included in the NDC Directory?

    Yes, Plexion with product code 57883-404 is active and included in the NDC Directory. The product was first marketed by Brava Pharmaceuticals, Llc on September 01, 2005 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 57883-404-10?

    The 11-digit format is 57883040410. 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
    5-3-257883-404-105-4-257883-0404-10