NDC Package 68001-413-06 Duloxetine

View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

68001-413-06

Package Description:

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Product Code:

68001-413

Proprietary Name:

Duloxetine

Usage Information:

Duloxetine delayed-release capsules are indicated for the treatment of:•Major Depressive Disorder [see Clinical Studies (14.1)]•Generalized Anxiety Disorder [see Clinical Studies (14.2)]•Diabetic Peripheral Neuropathy [see Clinical Studies (14.3)]•Chronic Musculoskeletal Pain [see Clinical Studies (14.5)]

11-Digit NDC Billing Format:

68001041306

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

60 EA

NDC to RxNorm Crosswalk:

RxCUI: 596926 - DULoxetine 20 MG Delayed Release Oral Capsule
RxCUI: 596926 - duloxetine 20 MG Delayed Release Oral Capsule
RxCUI: 596926 - duloxetine 20 MG (as duloxetine HCl 22.4 MG) Delayed Release Oral Capsule
RxCUI: 596930 - DULoxetine 30 MG Delayed Release Oral Capsule
RxCUI: 596930 - duloxetine 30 MG Delayed Release Oral Capsule

Labeler Name:

Bluepoint

Sample Package:

FDA Application Number:

ANDA090778

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

09-30-2019

End Marketing Date:

04-30-2025

Listing Expiration Date:

04-30-2025

Exclude Flag:

Code Structure:

68001 - Bluepoint
- 68001-413 - Duloxetine
  - 68001-413-06 - 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE

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 68001-413-06?

The NDC Packaged Code 68001-413-06 is assigned to a package of 60 capsule, delayed release in 1 bottle of Duloxetine, labeled by Bluepoint. The product's dosage form is and is administered via form.

Is NDC 68001-413 included in the NDC Directory?

No, Duloxetine with product code 68001-413 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Bluepoint on September 30, 2019 and its listing in the NDC Directory is set to expire on April 30, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 68001-413-06?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 60.

What is the 11-digit format for NDC 68001-413-06?

The 11-digit format is 68001041306. 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 5-3-2 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	68001-413-06	5-4-2	68001-0413-06

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