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  5. NDC Package Code: 58118-3156-8 Buprenorphine

NDC Package 58118-3156-8 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:
58118-3156-8
Package Description:
30 TABLET in 1 BLISTER PACK
Product Code:
58118-3156
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:
58118315608
NDC to RxNorm Crosswalk:
  • RxCUI: 351264 - buprenorphine HCl 2 MG Sublingual Tablet
  • RxCUI: 351264 - buprenorphine 2 MG Sublingual Tablet
  • RxCUI: 351264 - buprenorphine 2 MG (as buprenorphine HCl 2.16 MG) Sublingual Tablet
    • Labeler Name:
    Clinical Solutions Wholesale, Llc
    Sample Package:
    No
    Start Marketing Date:
    02-19-2015
    Listing Expiration Date:
    12-31-2020
    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 58118-3156-8?

    The NDC Packaged Code 58118-3156-8 is assigned to a package of 30 tablet in 1 blister pack of Buprenorphine, labeled by Clinical Solutions Wholesale, Llc. The product's dosage form is and is administered via form.

    Is NDC 58118-3156 included in the NDC Directory?

    No, Buprenorphine with product code 58118-3156 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Clinical Solutions Wholesale, Llc on February 19, 2015 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 58118-3156-8?

    The 11-digit format is 58118315608. 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
    5-4-158118-3156-85-4-258118-3156-08