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  5. NDC Package Code: 71335-2567-6 Duloxetine

NDC Package 71335-2567-6 Duloxetine

Capsule, Delayed Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

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:
71335-2567-6
Package Description:
120 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Code:
71335-2567
Proprietary Name:
Duloxetine
Non-Proprietary Name:
Duloxetine
Substance Name:
Duloxetine Hydrochloride
11-Digit NDC Billing Format:
71335256706
NDC to RxNorm Crosswalk:
  • RxCUI: 596934 - DULoxetine 60 MG Delayed Release Oral Capsule
  • RxCUI: 596934 - duloxetine 60 MG Delayed Release Oral Capsule
  • RxCUI: 596934 - duloxetine 60 MG (as duloxetine HCl 67.3 MG) Delayed Release Oral Capsule
Product Type:
Human Prescription Drug
Labeler Name:
Bryant Ranch Prepack
Dosage Form:
Capsule, Delayed Release - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin, and which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
DULOXETINE HYDROCHLORIDE 60 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA090694
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
12-11-2013
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
71335-2567-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE
71335-2567-228 CAPSULE, DELAYED RELEASE in 1 BOTTLE
71335-2567-360 CAPSULE, DELAYED RELEASE in 1 BOTTLE
71335-2567-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE
71335-2567-5180 CAPSULE, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 71335-2567-6?

The NDC Packaged Code 71335-2567-6 is assigned to a package of 120 capsule, delayed release in 1 bottle of Duloxetine, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is capsule, delayed release and is administered via oral form.

Is NDC 71335-2567 included in the NDC Directory?

Yes, Duloxetine with product code 71335-2567 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on December 11, 2013 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71335-2567-6?

The 11-digit format is 71335256706. 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
5-4-171335-2567-65-4-271335-2567-06