NDC Package 50844-930-10 Menstrual Complete Maximum Strength

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:
50844-930-10
Package Description:
1 BOTTLE in 1 CARTON / 40 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Menstrual Complete Maximum Strength
Non-Proprietary Name:
Acetaminophen, Caffeine, Pyrilamine Maleate
Substance Name:
Acetaminophen; Caffeine; Pyrilamine Maleate
Usage Information:
Do not take more than the recommended dose adults and children 12 years and over: take 2 caplets with water repeat every 6 hours, as needed do not exceed 6 caplets per day children under 12 years: ask a doctor
11-Digit NDC Billing Format:
50844093010
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:
    L.n.k. International, Inc.
    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:
    12-31-2024
    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 50844-930-10?

    The NDC Packaged Code 50844-930-10 is assigned to a package of 1 bottle in 1 carton / 40 tablet, film coated in 1 bottle of Menstrual Complete Maximum Strength, a human over the counter drug labeled by L.n.k. International, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 50844-930 included in the NDC Directory?

    Yes, Menstrual Complete Maximum Strength with product code 50844-930 is active and included in the NDC Directory. The product was first marketed by L.n.k. International, Inc. on April 29, 2002 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 50844-930-10?

    The 11-digit format is 50844093010. 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
    5-3-250844-930-105-4-250844-0930-10