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  5. NDC Package Code: 16590-878-30 Reprexain

NDC Package 16590-878-30 Reprexain

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:
16590-878-30
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
16590-878
Proprietary Name:
Reprexain
Usage Information:
INDICATIONS AND USAGECarefully consider the potential benefits and risks of REPREXAIN™ and other treatment options before deciding to use REPREXAIN™. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS). REPREXAIN™ tablets are indicated for the short-term (generally less than 10 days) management of acute pain. REPREXAIN™ is not indicated for the treatment of such conditions as osteoarthritis or rheumatoid arthritis.
11-Digit NDC Billing Format:
16590087830
NDC to RxNorm Crosswalk:
  • RxCUI: 858778 - HYDROcodone bitartrate 5 MG / ibuprofen 200 MG Oral Tablet
  • RxCUI: 858778 - hydrocodone bitartrate 5 MG / ibuprofen 200 MG Oral Tablet
  • RxCUI: 858784 - REPREXAIN 5 MG / 200 MG Oral Tablet
  • RxCUI: 858784 - hydrocodone bitartrate 5 MG / ibuprofen 200 MG Oral Tablet [Reprexain]
  • RxCUI: 858784 - Reprexain 5/200 (hydrocodone / ibuprofen) Oral Tablet
    • Labeler Name:
    Stat Rx Usa
    Sample Package:
    No
    Start Marketing Date:
    12-16-2008
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    16590-878-2020 TABLET, FILM COATED in 1 BOTTLE
    16590-878-4040 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 16590-878-30?

    The NDC Packaged Code 16590-878-30 is assigned to a package of 30 tablet, film coated in 1 bottle of Reprexain, labeled by Stat Rx Usa. The product's dosage form is and is administered via form.

    Is NDC 16590-878 included in the NDC Directory?

    No, Reprexain with product code 16590-878 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Stat Rx Usa on December 16, 2008 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 16590-878-30?

    The 11-digit format is 16590087830. 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
    5-3-216590-878-305-4-216590-0878-30