NDC Package 59011-109-20 Oxycontin

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory .

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:
59011-109-20
Package Description:
2 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Oxycontin
Usage Information:
This medication is used to help relieve severe ongoing pain (such as due to cancer). Oxycodone 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. The higher strengths of this drug (more than 40 milligrams per tablet) should be used only if you have been regularly taking moderate to large amounts of an opioid pain medication. These strengths may cause overdose (even death) if taken by a person who has not been regularly taking opioids. Do not use the extended-release form of oxycodone to relieve pain that is mild or that will go away in a few days. This medication is not for occasional ("as needed") use.
11-Digit NDC Billing Format:
59011010920
Labeler Name:
Purdue Pharma Lp
Sample Package:
No
FDA Application Number:
NDA020553
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
01-01-1997
End Marketing Date:
05-31-2013
Listing Expiration Date:
05-31-2013
Exclude Flag:
D
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
59011-109-10100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 59011-109-20?

The NDC Packaged Code 59011-109-20 is assigned to a package of 2 blister pack in 1 carton / 10 tablet, film coated, extended release in 1 blister pack of Oxycontin, labeled by Purdue Pharma Lp. The product's dosage form is and is administered via form.

Is NDC 59011-109 included in the NDC Directory?

The product was first marketed by Purdue Pharma Lp on January 01, 1997 and its listing in the NDC Directory is set to expire on May 31, 2013 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 59011-109-20?

The 11-digit format is 59011010920. 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
5-3-259011-109-205-4-259011-0109-20