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  5. NDC Package Code: 50090-5805-0 Buprenorphine

NDC Package 50090-5805-0 Buprenorphine

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:
50090-5805-0
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
50090-5805
Proprietary Name:
Buprenorphine
Usage Information:
This medication is used to help relieve severe ongoing pain (such as due to arthritis, chronic back pain). Buprenorphine belongs to a class of drugs known as opioid analgesics. It works in the brain to change how your body feels and responds to pain. The higher strengths of this drug (7.5, 10, 15, or 20 micrograms per hour patches) should be used only if you have been regularly taking moderate amounts of opioid pain medication. These strengths may cause overdose (even death) if used by a person who has not been regularly taking opioids. Do not use this medication to relieve pain that is mild or that will go away in a few days. This medication is not for occasional ("as needed") use.
11-Digit NDC Billing Format:
50090580500
NDC to RxNorm Crosswalk:
  • RxCUI: 351265 - buprenorphine HCl 8 MG Sublingual Tablet
  • RxCUI: 351265 - buprenorphine 8 MG Sublingual Tablet
  • RxCUI: 351265 - buprenorphine 8 MG (as buprenorphine HCl 8.64 MG) Sublingual Tablet
    • Labeler Name:
    A-s Medication Solutions
    Sample Package:
    No
    Start Marketing Date:
    10-25-2017
    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 50090-5805-0?

    The NDC Packaged Code 50090-5805-0 is assigned to a package of 30 tablet in 1 bottle of Buprenorphine, labeled by A-s Medication Solutions. The product's dosage form is and is administered via form.

    Is NDC 50090-5805 included in the NDC Directory?

    No, Buprenorphine with product code 50090-5805 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 October 25, 2017 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 50090-5805-0?

    The 11-digit format is 50090580500. 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
    5-4-150090-5805-05-4-250090-5805-00