Mayzent Tablet, Film Coated
NDC Package 0078-1014-93
Package Information
Mayzent (siponimod) tablets is a medication used to treat a certain type of multiple sclerosis (relapsing multiple sclerosis-MS). This formulation utilizes a tablet, film coated delivery system. Marketed by Novartis Pharmaceuticals Corporation, this product is identified by NDC 0078-1014 and is authorized under FDA application NDA209884.
Identification & Billing
- RxCUI: 2121090 - siponimod 0.25 MG Oral Tablet
- RxCUI: 2121096 - MAYZENT 0.25 MG Oral Tablet
- RxCUI: 2121096 - siponimod 0.25 MG Oral Tablet [Mayzent]
- RxCUI: 2121096 - Mayzent 0.25 MG Oral Tablet
- RxCUI: 2121098 - siponimod 2 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0078 - Novartis Pharmaceuticals Corporation
- 0078-1014 - Mayzent
- 0078-1014-93 - 30 TABLET, FILM COATED in 1 BOTTLE
- 0078-1014 - Mayzent
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 (0078-1014). 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 0078-1014-93 identifies a specific commercial package of 30 tablet, film coated in 1 bottle of Mayzent, a human prescription drug labeled by Novartis Pharmaceuticals Corporation. This tablet, film coated is formulated for oral use and contains siponimod 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 Novartis Pharmaceuticals Corporation on March 26, 2019. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
This medication is used to treat a certain type of multiple sclerosis (relapsing multiple sclerosis-MS). Siponimod is not a cure for MS but it is thought to help by preventing immune system cells (lymphocytes) from attacking the nerves in your brain and spinal cord. It helps decrease the number of episodes of disease worsening (relapses) and may prevent or delay disability.
How is this Novartis Pharmaceuticals Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00078101493. 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 Labeler segment to maintain the 5-4-2 structure.