1. Home
  2. Labeler Index
  3. Halo Pharmaceutical Inc
  4. 72022-582
  5. NDC Package Code: 72022-582-01 Oxycodone And Acetaminophen

NDC Package 72022-582-01 Oxycodone And Acetaminophen

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:
72022-582-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
72022-582
Proprietary Name:
Oxycodone And Acetaminophen
Usage Information:
Oxycodone and Acetaminophen Tablets USP is indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate.Limitations of UseBecause of the risks of addiction, abuse, and misuse, with opioids, even at recommended doses [see WARNINGS], reserve Oxycodone and Acetaminophen Tablets for use in patients for whom alternative treatment options [e.g., non-opioid analgesics]Have not been tolerated, or are not expected to be tolerated,Have not provided adequate analgesia, or are not expected to provide adequate analgesia
11-Digit NDC Billing Format:
72022058201
NDC to RxNorm Crosswalk:
  • RxCUI: 1049214 - oxyCODONE 10 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 1049214 - acetaminophen 325 MG / oxycodone hydrochloride 10 MG Oral Tablet
  • RxCUI: 1049214 - APAP 325 MG / oxycodone hydrochloride 10 MG Oral Tablet
  • RxCUI: 1049221 - oxyCODONE 5 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 1049221 - acetaminophen 325 MG / oxycodone hydrochloride 5 MG Oral Tablet
    • Labeler Name:
    Halo Pharmaceutical Inc
    Sample Package:
    No
    Start Marketing Date:
    02-15-2020
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    72022-582-05500 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 72022-582-01?

    The NDC Packaged Code 72022-582-01 is assigned to a package of 100 tablet in 1 bottle of Oxycodone And Acetaminophen, labeled by Halo Pharmaceutical Inc. The product's dosage form is and is administered via form.

    Is NDC 72022-582 included in the NDC Directory?

    No, Oxycodone And Acetaminophen with product code 72022-582 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Halo Pharmaceutical Inc on February 15, 2020 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 72022-582-01?

    The 11-digit format is 72022058201. 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 5-3-2 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
    5-3-272022-582-015-4-272022-0582-01