NDC Package 67296-1040-2 Oxycodone Hydrochloride

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
67296-1040-2
Package Description:
20 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Oxycodone Hydrochloride
Non-Proprietary Name:
Oxycodone Hydrochloride
Substance Name:
Oxycodone Hydrochloride
Usage Information:
Oxycodone hydrochloride tablets are 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 AND PRECAUTIONS (5.1)], reserve oxycodone hydrochloride tablets for use in patients for whom alternative treatment options (e.g., non-opioid analgesics or opioid combination products):• 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:
67296104002
NDC to RxNorm Crosswalk:
  • RxCUI: 1049621 - oxyCODONE HCl 5 MG Oral Tablet
  • RxCUI: 1049621 - oxycodone hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Redpharm Drug, Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA090659
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-12-2009
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    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
    67296-1040-440 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67296-1040-2?

    The NDC Packaged Code 67296-1040-2 is assigned to a package of 20 tablet in 1 bottle of Oxycodone Hydrochloride, a human prescription drug labeled by Redpharm Drug, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 67296-1040 included in the NDC Directory?

    Yes, Oxycodone Hydrochloride with product code 67296-1040 is active and included in the NDC Directory. The product was first marketed by Redpharm Drug, Inc. on May 12, 2009 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67296-1040-2?

    The 11-digit format is 67296104002. 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
    5-4-167296-1040-25-4-267296-1040-02