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  5. NDC Package Code: 71335-0981-4 Oxycodone Hydrochloride

NDC Package 71335-0981-4 Oxycodone Hydrochloride

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:
71335-0981-4
Package Description:
56 TABLET in 1 BOTTLE
Product Code:
71335-0981
Proprietary Name:
Oxycodone Hydrochloride
Usage Information:
Oxycodone hydrochloride (HCl) 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 HCl 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:
71335098104
NDC to RxNorm Crosswalk:
  • RxCUI: 1049621 - oxyCODONE HCl 5 MG Oral Tablet
  • RxCUI: 1049621 - oxycodone hydrochloride 5 MG Oral Tablet
    • Labeler Name:
    Bryant Ranch Prepack
    Sample Package:
    No
    Start Marketing Date:
    10-30-2012
    Listing Expiration Date:
    12-31-2023
    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
    71335-0981-130 TABLET in 1 BOTTLE
    71335-0981-260 TABLET in 1 BOTTLE
    71335-0981-390 TABLET in 1 BOTTLE
    71335-0981-5100 TABLET in 1 BOTTLE
    71335-0981-6120 TABLET in 1 BOTTLE
    71335-0981-750 TABLET in 1 BOTTLE
    71335-0981-840 TABLET in 1 BOTTLE
    71335-0981-920 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71335-0981-4?

    The NDC Packaged Code 71335-0981-4 is assigned to a package of 56 tablet in 1 bottle of Oxycodone Hydrochloride, labeled by Bryant Ranch Prepack. The product's dosage form is and is administered via form.

    Is NDC 71335-0981 included in the NDC Directory?

    No, Oxycodone Hydrochloride with product code 71335-0981 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Bryant Ranch Prepack on October 30, 2012 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71335-0981-4?

    The 11-digit format is 71335098104. 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
    5-4-171335-0981-45-4-271335-0981-04