Desvenlafaxine Tablet, Extended Release
NDC Package 10135-821-10
Package Information
Desvenlafaxine tablets is desvenlafaxine is used to treat depression. This formulation utilizes a tablet, extended release delivery system. Marketed by Marlex Pharmaceuticals, Inc., this product is identified by NDC 10135-821 and is authorized under FDA application ANDA204805.
Identification & Billing
- RxCUI: 1874553 - desvenlafaxine succinate 100 MG 24HR Extended Release Oral Tablet
- RxCUI: 1874553 - 24 HR desvenlafaxine succinate 100 MG Extended Release Oral Tablet
- RxCUI: 1874553 - desvenlafaxine 100 MG (as desvenlafaxine succinate 152 MG) 24HR Extended Release Oral Tablet
- RxCUI: 1874559 - desvenlafaxine succinate 50 MG 24HR Extended Release Oral Tablet
- RxCUI: 1874559 - 24 HR desvenlafaxine succinate 50 MG Extended Release Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 10135 - Marlex Pharmaceuticals, Inc.
- 10135-821 - Desvenlafaxine
- 10135-821-10 - 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 10135-821 - Desvenlafaxine
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 (10135-821). Click a package code to view its specific billing and regulatory data.
* 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 10135-821-10 identifies a specific commercial package of 1000 tablet, extended release in 1 bottle of Desvenlafaxine, a human prescription drug labeled by Marlex Pharmaceuticals, Inc.. This tablet, extended release is formulated for oral use and contains desvenlafaxine succinate as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Marlex Pharmaceuticals, Inc. on July 01, 2025. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Desvenlafaxine is used to treat depression. It may improve your mood, feelings of well-being, and energy level. Desvenlafaxine is known as a serotonin-norepinephrine reuptake inhibitor (SNRI). It works by helping to restore the balance of certain natural substances (serotonin and norepinephrine) in the brain.
How is this Marlex Pharmaceuticals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 10135082110. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.