NDC Package 67296-1705-6 Hydrocodone Bitartrate And Acetaminophen

View Billable Units, 11-Digit Format, RxNorm

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:
67296-1705-6
Package Description:
6 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Hydrocodone Bitartrate And Acetaminophen
Usage Information:
Hydrocodone bitartrate and acetaminophen tablets, USP 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], reserve hydrocodone bitartrate and acetaminophen tablets, USP 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:
67296170506
NDC to RxNorm Crosswalk:
  • RxCUI: 857005 - HYDROcodone bitartrate 7.5 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 857005 - acetaminophen 325 MG / hydrocodone bitartrate 7.5 MG Oral Tablet
  • RxCUI: 857005 - APAP 325 MG / hydrocodone bitartrate 7.5 MG Oral Tablet
  • Labeler Name:
    Redpharm Drug, Inc.
    Sample Package:
    No
    Start Marketing Date:
    11-01-2019
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I

    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
    67296-1705-330 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67296-1705-6?

    The NDC Packaged Code 67296-1705-6 is assigned to a package of 6 tablet in 1 bottle of Hydrocodone Bitartrate And Acetaminophen, labeled by Redpharm Drug, Inc.. The product's dosage form is and is administered via form.

    Is NDC 67296-1705 included in the NDC Directory?

    No, Hydrocodone Bitartrate And Acetaminophen with product code 67296-1705 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Redpharm Drug, Inc. on November 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67296-1705-6?

    The 11-digit format is 67296170506. 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
    5-4-167296-1705-65-4-267296-1705-06