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  5. NDC Package Code: 50771-203-02 Duloxetine Hydrochloride

NDC Package 50771-203-02 Duloxetine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
50771-203-02
Package Description:
500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC
Product Code:
50771-203
Proprietary Name:
Duloxetine Hydrochloride
Usage Information:
Duloxetine delayed-release capsules, USP 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:
50771020302
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:
    Yaopharma Co., Ltd.
    Sample Package:
    No
    Start Marketing Date:
    01-01-2024
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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
    50771-203-0130 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50771-203-02?

    The NDC Packaged Code 50771-203-02 is assigned to a package of 500 capsule, delayed release pellets in 1 bottle, plastic of Duloxetine Hydrochloride, labeled by Yaopharma Co., Ltd.. The product's dosage form is and is administered via form.

    Is NDC 50771-203 included in the NDC Directory?

    No, Duloxetine Hydrochloride with product code 50771-203 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Yaopharma Co., Ltd. on January 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50771-203-02?

    The 11-digit format is 50771020302. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-250771-203-025-4-250771-0203-02