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  5. NDC Package Code: 55154-2579-0 Duloxetine

NDC Package 55154-2579-0 Duloxetine

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
55154-2579-0
Package Description:
10 BLISTER PACK in 1 BAG / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product Code:
55154-2579
Proprietary Name:
Duloxetine
Usage Information:
Duloxetine delayed-release capsules are indicated for the treatment of:•Major depressive disorder in adults•Generalized anxiety disorder in adults and pediatric patients 7 years of age and older•Diabetic peripheral neuropathic pain in adults•Fibromyalgia in adults•Chronic musculoskeletal pain in adultsAdditional pediatric use information is approved for Eli Lilly and Company, Inc.’s CYMBALTA (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company Inc.’s marketing exclusivity rights, this drug product is not labeled with that pediatric information.
11-Digit NDC Billing Format:
55154257900
Labeler Name:
Cardinal Health 107, Llc
Sample Package:
No
FDA Application Number:
ANDA090778
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-01-2023
End Marketing Date:
02-01-2023
Listing Expiration Date:
02-01-2023
Exclude Flag:
D
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 55154-2579-0?

The NDC Packaged Code 55154-2579-0 is assigned to a package of 10 blister pack in 1 bag / 1 capsule, delayed release in 1 blister pack of Duloxetine, labeled by Cardinal Health 107, Llc. The product's dosage form is and is administered via form.

Is NDC 55154-2579 included in the NDC Directory?

No, Duloxetine with product code 55154-2579 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Cardinal Health 107, Llc on February 01, 2023 and its listing in the NDC Directory is set to expire on February 01, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 55154-2579-0?

The 11-digit format is 55154257900. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-155154-2579-05-4-255154-2579-00