Asciminib Tablet, Film Coated
NDC Package 17088-0163-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Asciminib tablets is a human prescription drug. This formulation utilizes a tablet, film coated delivery system. Marketed by Novartis Pharma Stein Ag, this product is identified by NDC 17088-0163.

Identification & Billing

NDC Package Code
17088-0163-1
Package Description
25000 TABLET, FILM COATED in 1 DRUM
Product Code
17088-0163
11-Digit Billing Format
17088016301

Clinical Specifications

Proprietary Name
Asciminib
Non-Proprietary Name
Asciminib
Substance Name
Asciminib Hydrochloride
Dosage Form
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Active Ingredient(s)
ASCIMINIB HYDROCHLORIDE 40 mg/1

Regulatory & Marketing

Labeler Name
Novartis Pharma Stein Ag
Product Type
Human Prescription Drug
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
10-29-2021
Listing Expiration
12-31-2027
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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 17088-0163-1 identifies a specific commercial package of 25000 tablet, film coated in 1 drum of Asciminib (UNFINISHED drug), a human prescription drug labeled by Novartis Pharma Stein Ag. This tablet, film coated is formulated for use and contains asciminib hydrochloride 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 Pharma Stein Ag on October 29, 2021. The current certification is valid through December 31, 2027.

How is this Novartis Pharma Stein Ag product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 17088016301. 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 (5-4-1)
17088-0163-1
11-Digit CMS (5-4-2)
17088-0163-01

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