NDC Package 69676-0063-5 Genexa Acetaminophen Pm Extra Strength

Acetaminophen Tablet, 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:
69676-0063-5
Package Description:
1 BOTTLE in 1 CARTON / 50 TABLET, COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Genexa Acetaminophen Pm Extra Strength
Non-Proprietary Name:
Acetaminophen
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride
Usage Information:
This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.
11-Digit NDC Billing Format:
69676006305
NDC to RxNorm Crosswalk:
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1092189 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Genexa Inc.
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-17-2022
    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
    69676-0063-21 BOTTLE in 1 CARTON / 100 TABLET, COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69676-0063-5?

    The NDC Packaged Code 69676-0063-5 is assigned to a package of 1 bottle in 1 carton / 50 tablet, coated in 1 bottle of Genexa Acetaminophen Pm Extra Strength, a human over the counter drug labeled by Genexa Inc.. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 69676-0063 included in the NDC Directory?

    Yes, Genexa Acetaminophen Pm Extra Strength with product code 69676-0063 is active and included in the NDC Directory. The product was first marketed by Genexa Inc. on February 17, 2022 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 69676-0063-5?

    The 11-digit format is 69676006305. 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
    5-4-169676-0063-55-4-269676-0063-05