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  5. NDC Package Code: 72275-718-77 Fluovix Plus

NDC Package 72275-718-77 Fluovix Plus

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:
72275-718-77
Package Description:
1 PACKAGE in 1 CARTON / 1 TUBE in 1 PACKAGE / 1 KIT in 1 TUBE * 1 TUBE in 1 CARTON / 120 g in 1 TUBE
Product Code:
72275-718
Proprietary Name:
Fluovix Plus
Usage Information:
Instructions for UseClean and dry the affected area.Gently apply a thin film--1-2 grams, 1-2 times daily or as directed by your physician.Do not apply over a large area of skin.Thoroughly wash and dry hands before the next step.Roll out Soft Silicone to the desired length, tear at the perforated line and then remove adhesive backing.Place Soft Silicone onto the affected area, and gently apply pressure around the edges for complete coverage.Use the Soft Silicone tape in conjuction with Fluocinonide Cream 0.1%, only as directed by your physician.
11-Digit NDC Billing Format:
72275071877
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 485647 - fluocinonide 0.1 % Topical Cream
  • RxCUI: 485647 - fluocinonide 1 MG/ML Topical Cream
  • RxCUI: 485647 - fluocinonide 1 MG per 1 GM Topical Cream
    • Labeler Name:
    Primary Pharmaceuticals, Inc.
    Sample Package:
    No
    Start Marketing Date:
    11-05-2019
    Listing Expiration Date:
    12-31-2022
    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 72275-718-77?

    The NDC Packaged Code 72275-718-77 is assigned to a package of 1 package in 1 carton / 1 tube in 1 package / 1 kit in 1 tube * 1 tube in 1 carton / 120 g in 1 tube of Fluovix Plus, labeled by Primary Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

    Is NDC 72275-718 included in the NDC Directory?

    No, Fluovix Plus with product code 72275-718 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Primary Pharmaceuticals, Inc. on November 05, 2019 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 72275-718-77?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

    What is the 11-digit format for NDC 72275-718-77?

    The 11-digit format is 72275071877. 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
    5-3-272275-718-775-4-272275-0718-77