Tramadol Hydrochloride
NDC Package 45865-709-30

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

Tramadol Hydrochloride is extended-Release is indicated for the management of moderate to moderately severe chronic pain in adults who require around-the-clock treatment of their pain for an extended period of time. Marketed by Medsource Pharmaceuticals, this product is identified by NDC 45865-709 and is authorized under FDA application NDA022370.

Identification & Billing

NDC Package Code
45865-709-30
Package Description
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Code
45865-709
11-Digit Billing Format
45865070930
RxNorm Crosswalk
  • RxCUI: 1248115 - traMADol HCl 150 MG 24HR Extended Release Oral Capsule
  • RxCUI: 1248115 - 24 HR tramadol hydrochloride 150 MG Extended Release Oral Capsule
  • RxCUI: 1248115 - tramadol HCl 150 MG 24 HR Extended Release Oral Capsule

Clinical Specifications

Proprietary Name
Tramadol Hydrochloride
Dosage Form
-
Usage Information
Tramadol Hydrochloride Extended-Release is indicated for the management of moderate to moderately severe chronic pain in adults who require around-the-clock treatment of their pain for an extended period of time.

Regulatory & Marketing

Labeler Name
Medsource Pharmaceuticals
FDA Application #
NDA022370
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
03-14-2012
Listing Expiration
12-31-2024
Exclude Flag
I
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (45865-709). Click a package code to view its specific billing and regulatory data.

45865-709-60
60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE

* 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 45865-709-30 identifies a specific commercial package of 30 capsule, extended release in 1 bottle of Tramadol Hydrochloride, labeled by Medsource 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 Medsource Pharmaceuticals on March 14, 2012. The current certification is valid through December 31, 2024.

How is this Medsource Pharmaceuticals product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 45865070930. 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)
45865-709-30
11-Digit CMS (5-4-2)
45865-0709-30

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