NDC Package 41163-956-09 Acetaminophen Pm Extra Strength

Acetaminophen,Diphenhydramine Hcl 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:
41163-956-09
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 20 TABLET, COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Acetaminophen Pm Extra Strength
Non-Proprietary Name:
Acetaminophen, Diphenhydramine Hcl
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride
Usage Information:
Do not take more than directedadults and children 12 years and overtake 2 gelcaps at bedtimedo not take more than 2 gelcaps of this product in 24 hourschildren under 12 years: do not useĀ 
11-Digit NDC Billing Format:
41163095609
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:
    United Natural Foods, Inc. Dba Unfi
    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:
    12-17-2007
    Listing Expiration Date:
    12-31-2025
    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 41163-956-09?

    The NDC Packaged Code 41163-956-09 is assigned to a package of 1 bottle, plastic in 1 carton / 20 tablet, coated in 1 bottle, plastic of Acetaminophen Pm Extra Strength, a human over the counter drug labeled by United Natural Foods, Inc. Dba Unfi. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 41163-956 included in the NDC Directory?

    Yes, Acetaminophen Pm Extra Strength with product code 41163-956 is active and included in the NDC Directory. The product was first marketed by United Natural Foods, Inc. Dba Unfi on December 17, 2007 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 41163-956-09?

    The 11-digit format is 41163095609. 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
    5-3-241163-956-095-4-241163-0956-09