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  5. NDC Package Code: 67296-0041-2 Acetaminophen And Codeine Phosphate

NDC Package 67296-0041-2 Acetaminophen And Codeine Phosphate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
67296-0041-2
Package Description:
20 TABLET in 1 BOTTLE
Product Code:
67296-0041
Proprietary Name:
Acetaminophen And Codeine Phosphate
Usage Information:
Lorazepam is indicated for the management of anxiety disorders or for the short-term relief of the symptoms of anxiety or anxiety associated with depressive symptoms. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic.The effectiveness of lorazepam in long-term use, that is, more than 4 months, has not been assessed by systematic clinical studies. The physician should periodically reassess the usefulness of the drug for the individual patient.
11-Digit NDC Billing Format:
67296004102
NDC to RxNorm Crosswalk:
  • RxCUI: 993770 - codeine phosphate 15 MG / acetaminophen 300 MG Oral Tablet
  • RxCUI: 993770 - acetaminophen 300 MG / codeine phosphate 15 MG Oral Tablet
  • RxCUI: 993770 - APAP 300 MG / codeine phosphate 15 MG Oral Tablet
    • Labeler Name:
    Redpharm Drug Inc.
    Sample Package:
    No
    Start Marketing Date:
    10-07-2010
    Listing Expiration Date:
    12-31-2017
    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.

    Frequently Asked Questions

    What is NDC 67296-0041-2?

    The NDC Packaged Code 67296-0041-2 is assigned to a package of 20 tablet in 1 bottle of Acetaminophen And Codeine Phosphate, labeled by Redpharm Drug Inc.. The product's dosage form is and is administered via form.

    Is NDC 67296-0041 included in the NDC Directory?

    No, Acetaminophen And Codeine Phosphate with product code 67296-0041 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 October 07, 2010 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67296-0041-2?

    The 11-digit format is 67296004102. 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
    5-4-167296-0041-25-4-267296-0041-02