NDC Package 50090-3811-0 Methylprednisolone

View Billable Units, 11-Digit Format, RxNorm

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:
50090-3811-0
Package Description:
1 BLISTER PACK in 1 CARTON / 21 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Methylprednisolone
Usage Information:
Methylprednisolone is used to treat conditions such as arthritis, blood disorders, severe allergic reactions, certain cancers, eye conditions, skin/kidney/intestinal/lung diseases, and immune system disorders. It decreases your immune system's response to various diseases to reduce symptoms such as swelling, pain, and allergic-type reactions. This medication is a corticosteroid hormone. Methylprednisolone may also be used with other medications in hormone disorders.
11-Digit NDC Billing Format:
50090381100
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 259966 - methylPREDNISolone 4 MG Oral Tablet
  • RxCUI: 259966 - methylprednisolone 4 MG Oral Tablet
  • RxCUI: 762675 - {21 (methylprednisolone 4 MG Oral Tablet) } Pack
  • RxCUI: 762675 - methylPREDNISolone 4 MG Tablet 6 Day 21 Count Pack
  • RxCUI: 762675 - methylprednisolone 4 MG Oral Tablet 21 Count Pack
  • Labeler Name:
    A-s Medication Solutions
    Sample Package:
    No
    Start Marketing Date:
    05-01-2018
    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 50090-3811-0?

    The NDC Packaged Code 50090-3811-0 is assigned to a package of 1 blister pack in 1 carton / 21 tablet in 1 blister pack of Methylprednisolone, labeled by A-s Medication Solutions. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 50090-3811 included in the NDC Directory?

    No, Methylprednisolone with product code 50090-3811 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by A-s Medication Solutions on May 01, 2018 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 50090-3811-0?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 50090-3811-0?

    The 11-digit format is 50090381100. 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
    5-4-150090-3811-05-4-250090-3811-00