NDC Package 16590-747-30 Opana ER

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:
16590-747-30
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Opana ER
Usage Information:
Oxymorphone is used to help relieve moderate to severe pain. It belongs to a class of drugs known as opioid analgesics. It works in the brain to change how your body feels and responds to pain.
11-Digit NDC Billing Format:
16590074730
NDC to RxNorm Crosswalk:
  • RxCUI: 977874 - oxyMORphone HCl 10 MG 12HR Extended Release Oral Tablet
  • RxCUI: 977874 - 12 HR oxymorphone hydrochloride 10 MG Extended Release Oral Tablet
  • RxCUI: 977874 - oxymorphone hydrochloride 10 MG 12 HR Extended Release Oral Tablet
  • RxCUI: 977876 - OPANA ER 10 MG 12HR Extended Release Oral Tablet
  • RxCUI: 977876 - 12 HR oxymorphone hydrochloride 10 MG Extended Release Oral Tablet [Opana]
  • Labeler Name:
    Stat Rx Usa Llc
    Sample Package:
    No
    Start Marketing Date:
    06-22-2006
    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
    16590-747-5656 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    16590-747-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    16590-747-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 16590-747-30?

    The NDC Packaged Code 16590-747-30 is assigned to a package of 30 tablet, film coated, extended release in 1 bottle of Opana ER, labeled by Stat Rx Usa Llc. The product's dosage form is and is administered via form.

    Is NDC 16590-747 included in the NDC Directory?

    No, Opana ER with product code 16590-747 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Stat Rx Usa Llc on June 22, 2006 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 16590-747-30?

    The 11-digit format is 16590074730. 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
    5-3-216590-747-305-4-216590-0747-30