NDC Package 69117-0024-5 Paroxetine

Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

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:
69117-0024-5
Package Description:
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Paroxetine
Non-Proprietary Name:
Paroxetine
Substance Name:
Paroxetine Hydrochloride Hemihydrate
Usage Information:
Paroxetine is indicated in adults for the treatment of:Major depressive disorder (MDD)Obsessive compulsive disorder (OCD)Panic disorder (PD)Social anxiety disorder (SAD)Generalized anxiety disorder (GAD)Posttraumatic stress disorder (PTSD)
11-Digit NDC Billing Format:
69117002405
NDC to RxNorm Crosswalk:
  • RxCUI: 1738483 - PARoxetine HCl 10 MG Oral Tablet
  • RxCUI: 1738483 - paroxetine hydrochloride 10 MG Oral Tablet
  • RxCUI: 1738495 - PARoxetine HCl 20 MG Oral Tablet
  • RxCUI: 1738495 - paroxetine hydrochloride 20 MG Oral Tablet
  • RxCUI: 1738503 - PARoxetine HCl 30 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Yiling Pharmaceutical, Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA211248
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-02-2021
    Listing Expiration Date:
    12-31-2024
    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
    69117-0024-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    69117-0024-290 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    69117-0024-3100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    69117-0024-4500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69117-0024-5?

    The NDC Packaged Code 69117-0024-5 is assigned to a package of 1000 tablet, film coated in 1 bottle, plastic of Paroxetine, a human prescription drug labeled by Yiling Pharmaceutical, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 69117-0024 included in the NDC Directory?

    Yes, Paroxetine with product code 69117-0024 is active and included in the NDC Directory. The product was first marketed by Yiling Pharmaceutical, Inc. on November 02, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69117-0024-5?

    The 11-digit format is 69117002405. 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
    5-4-169117-0024-55-4-269117-0024-05