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  5. NDC Package Code: 55379-405-31 Hybrisil

NDC Package 55379-405-31 Hybrisil

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:
55379-405-31
Package Description:
1 BOTTLE, PUMP in 1 CARTON / 30 g in 1 BOTTLE, PUMP (55379-405-30)
Product Code:
55379-405
Proprietary Name:
Hybrisil
Usage Information:
HybriSil™ topical gel is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses, including those associated with the formation of scar tissue.
11-Digit NDC Billing Format:
55379040531
NDC to RxNorm Crosswalk:
  • RxCUI: 1100387 - methylPREDNISolone acetate 1 % Topical Gel
  • RxCUI: 1100387 - methylprednisolone acetate 0.01 MG/MG Topical Gel
  • RxCUI: 1100387 - methylprednisolone acetate 1 % Topical Gel
  • RxCUI: 1100391 - HybriSil 1 % Topical Gel
  • RxCUI: 1100391 - methylprednisolone acetate 0.01 MG/MG Topical Gel [HybriSil]
    • Labeler Name:
    Biozone Laboratories, Inc.
    Sample Package:
    No
    Start Marketing Date:
    05-05-2010
    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.

    Frequently Asked Questions

    What is NDC 55379-405-31?

    The NDC Packaged Code 55379-405-31 is assigned to a package of 1 bottle, pump in 1 carton / 30 g in 1 bottle, pump (55379-405-30) of Hybrisil, labeled by Biozone Laboratories, Inc.. The product's dosage form is and is administered via form.

    Is NDC 55379-405 included in the NDC Directory?

    No, Hybrisil with product code 55379-405 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Biozone Laboratories, Inc. on May 05, 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 55379-405-31?

    The 11-digit format is 55379040531. 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
    5-3-255379-405-315-4-255379-0405-31