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  5. NDC Package Code: 0363-0714-42 Extra Strength Nitetime Pain Relief

NDC Package 0363-0714-42 Extra Strength Nitetime Pain Relief

Acetaminophen 500 Mg, Diphenhydramine Hydrochloride 25 Mg Tablet Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
0363-0714-42
Package Description:
1 BOTTLE in 1 CARTON / 24 TABLET in 1 BOTTLE
Product Code:
0363-0714
Proprietary Name:
Extra Strength Nitetime Pain Relief
Non-Proprietary Name:
Acetaminophen 500 Mg, Diphenhydramine Hydrochloride 25 Mg Tablet
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride
Usage Information:
Uses temporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness
11-Digit NDC Billing Format:
00363071442
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:
    Walgreens
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 500 mg/1
  • DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
    • Pharmacologic Class(es):
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    part343
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    10-12-2021
    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.

    Frequently Asked Questions

    What is NDC 0363-0714-42?

    The NDC Packaged Code 0363-0714-42 is assigned to a package of 1 bottle in 1 carton / 24 tablet in 1 bottle of Extra Strength Nitetime Pain Relief, a human over the counter drug labeled by Walgreens. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0363-0714 included in the NDC Directory?

    Yes, Extra Strength Nitetime Pain Relief with product code 0363-0714 is active and included in the NDC Directory. The product was first marketed by Walgreens on October 12, 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 0363-0714-42?

    The 11-digit format is 00363071442. 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 4-4-2 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
    4-4-20363-0714-425-4-200363-0714-42