Atomoxetine Hydrochloride Capsule
NDC Package 0110-3239-10

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.

Atomoxetine Hydrochloride capsules is a drug for further processing. This formulation utilizes a capsule delivery system. Marketed by Lilly Del Caribe, Inc., this product is identified by NDC 0110-3239.

Identification & Billing

NDC Package Code
0110-3239-10
Package Description
105000 CAPSULE in 1 DRUM
Product Code
0110-3239
11-Digit Billing Format
00110323910

Clinical Specifications

Proprietary Name
Atomoxetine Hydrochloride
Non-Proprietary Name
Atomoxetine Hydrochloride
Substance Name
Atomoxetine Hydrochloride
Dosage Form
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Active Ingredient(s)
ATOMOXETINE HYDROCHLORIDE 60 mg/1

Regulatory & Marketing

Labeler Name
Lilly Del Caribe, Inc.
Product Type
Drug For Further Processing
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
11-26-2002
End Marketing Date
07-31-2027
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 0110-3239-10 identifies a specific commercial package of 105000 capsule in 1 drum of Atomoxetine Hydrochloride (UNFINISHED drug), drug for further processing labeled by Lilly Del Caribe, Inc.. This capsule is formulated for use and contains atomoxetine 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 Lilly Del Caribe, Inc. on November 26, 2002.

How is this Lilly Del Caribe, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00110323910. 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 (4-4-2)
0110-3239-10
11-Digit CMS (5-4-2)
00110-3239-10

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