NDC Package 0363-3900-22 Menstrual Pain Relief

Acetaminophen,Caffeine,Pyrilamine Maleate 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:
0363-3900-22
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 48 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Menstrual Pain Relief
Non-Proprietary Name:
Acetaminophen, Caffeine, Pyrilamine Maleate
Substance Name:
Acetaminophen; Caffeine; Pyrilamine Maleate
Usage Information:
Do not take more than the recommended doseadults and children 12 years and over:take 2 caplets with waterrepeat every 6 hours, as neededdo not exceed 6 caplets per daychildren under 12 years: ask a doctor
11-Digit NDC Billing Format:
00363390022
NDC to RxNorm Crosswalk:
  • RxCUI: 1597298 - acetaminophen 500 MG / caffeine 60 MG / pyrilamine maleate 15 MG Oral Tablet
  • RxCUI: 1597298 - APAP 500 MG / Caffeine 60 MG / Pyrilamine Maleate 15 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Walgreen Company
    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:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-29-2002
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0363-3900-101 BOTTLE, PLASTIC in 1 CARTON / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0363-3900-22?

    The NDC Packaged Code 0363-3900-22 is assigned to a package of 1 bottle, plastic in 1 carton / 48 tablet, film coated in 1 bottle, plastic of Menstrual Pain Relief, a human over the counter drug labeled by Walgreen Company. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 0363-3900 included in the NDC Directory?

    Yes, Menstrual Pain Relief with product code 0363-3900 is active and included in the NDC Directory. The product was first marketed by Walgreen Company on April 29, 2002 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 0363-3900-22?

    The 11-digit format is 00363390022. 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
    4-4-20363-3900-225-4-200363-3900-22