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  5. NDC Package Code: 73548-1039-1 Buprenorphine

NDC Package 73548-1039-1 Buprenorphine

Powder - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
73548-1039-1
Package Description:
10 kg in 1 DRUM
Product Code:
73548-1039
Non-Proprietary Name:
Buprenorphine
Substance 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:
73548103901
Product Type:
Bulk Ingredient
Labeler Name:
Purisys Llc
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s):
  • BUPRENORPHINE 1 kg/kg
    • DEA Schedule:
    Schedule III (CIII) Substances
    Sample Package:
    N/A
    Marketing Category:
    BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
    Start Marketing Date:
    07-14-2020
    End Marketing Date:
    07-31-2025
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    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 73548-1039-1?

    The NDC Packaged Code 73548-1039-1 is assigned to an UNFINISHED drug package of 10 kg in 1 drum of Buprenorphine, a bulk ingredient labeled by Purisys Llc. The product's dosage form is powder and is administered via form.

    Is NDC 73548-1039 included in the NDC Directory?

    Yes, Buprenorphine is an UNFINISHED PRODUCT with code 73548-1039 that is active and included in the NDC Directory. The product was first marketed by Purisys Llc on July 14, 2020.

    What is the 11-digit format for NDC 73548-1039-1?

    The 11-digit format is 73548103901. 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
    5-4-173548-1039-15-4-273548-1039-01