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  5. NDC Package Code: 50090-4333-1 Ibu

NDC Package 50090-4333-1 Ibu

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
50090-4333-1
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
50090-4333
Proprietary Name:
Ibu
Usage Information:
Ibuprofen is used to relieve pain from various conditions such as headache, dental pain, menstrual cramps, muscle aches, or arthritis. It is also used to reduce fever and to relieve minor aches and pain due to the common cold or flu. Ibuprofen is a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. This effect helps to decrease swelling, pain, or fever. If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.
11-Digit NDC Billing Format:
50090433301
NDC to RxNorm Crosswalk:
  • RxCUI: 197806 - ibuprofen 600 MG Oral Tablet
  • RxCUI: 206913 - Ibu 600 MG Oral Tablet
  • RxCUI: 206913 - ibuprofen 600 MG Oral Tablet [Ibu]
    • Labeler Name:
    A-s Medication Solutions
    Sample Package:
    No
    Start Marketing Date:
    11-20-2008
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50090-4333-030 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50090-4333-1?

    The NDC Packaged Code 50090-4333-1 is assigned to a package of 30 tablet in 1 bottle of Ibu, labeled by A-s Medication Solutions. The product's dosage form is and is administered via form.

    Is NDC 50090-4333 included in the NDC Directory?

    No, Ibu with product code 50090-4333 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 November 20, 2008 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 11-digit format for NDC 50090-4333-1?

    The 11-digit format is 50090433301. 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
    5-4-150090-4333-15-4-250090-4333-01