Primlev
NDC Package 59702-682-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Primlev is this combination medication is used to help relieve moderate to severe pain. Marketed by Atley Pharmaceuticals, this product is identified by NDC 59702-682 and is authorized under FDA application ANDA040608.

Identification & Billing

NDC Package Code
59702-682-01
Package Description
100 TABLET in 1 BOTTLE
Product Code
11-Digit Billing Format
59702068201

Clinical Specifications

Proprietary Name
Primlev
Dosage Form
-
Usage Information
This combination medication is used to help relieve moderate to severe pain. It contains a opioid pain reliever (oxycodone) and a non-opioid pain reliever (acetaminophen). Oxycodone works in the brain to change how your body feels and responds to pain. Acetaminophen can also reduce a fever.

Regulatory & Marketing

Labeler Name
Atley Pharmaceuticals
FDA Application #
ANDA040608
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
01-28-2010
End Marketing Date
12-03-2012
Listing Expiration
12-03-2012
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 59702-682-01 identifies a specific commercial package of 100 tablet in 1 bottle of Primlev, labeled by Atley Pharmaceuticals. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Atley Pharmaceuticals on January 28, 2010. The current certification is valid through December 03, 2012.

What are the primary indications for this medication?

This combination medication is used to help relieve moderate to severe pain. It contains a opioid pain reliever (oxycodone) and a non-opioid pain reliever (acetaminophen). Oxycodone works in the brain to change how your body feels and responds to pain. Acetaminophen can also reduce a fever.

How is this Atley Pharmaceuticals product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59702068201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
59702-682-01
11-Digit CMS (5-4-2)
59702-0682-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.