NDC Package 72036-171-02 Acetaminophen Pm

Acetaminophen And Diphenhydramine Hydrochloride 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:
72036-171-02
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 40 TABLET, COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Acetaminophen Pm
Non-Proprietary Name:
Acetaminophen And Diphenhydramine Hydrochloride
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride
Usage Information:
Do not take more than directed (see overdose warning) adults and children 12 years and overtake 2 gelcaps at bedtimedo not take more than 2 gelcaps of this product in 24 hourschildren under 12 yearsdo not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage
11-Digit NDC Billing Format:
72036017102
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:
    Harris Teeter
    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:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-06-2014
    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.

    Frequently Asked Questions

    What is NDC 72036-171-02?

    The NDC Packaged Code 72036-171-02 is assigned to a package of 1 bottle, plastic in 1 carton / 40 tablet, coated in 1 bottle, plastic of Acetaminophen Pm, a human over the counter drug labeled by Harris Teeter. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 72036-171 included in the NDC Directory?

    Yes, Acetaminophen Pm with product code 72036-171 is active and included in the NDC Directory. The product was first marketed by Harris Teeter on June 06, 2014 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 72036-171-02?

    The 11-digit format is 72036017102. 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
    5-3-272036-171-025-4-272036-0171-02