NDC Package 50580-230-07 Motrin Ib

Ibuprofen 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:
50580-230-07
Package Description:
1 BOTTLE in 1 CARTON / 24 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Motrin Ib
Non-Proprietary Name:
Ibuprofen
Substance Name:
Ibuprofen
Usage Information:
Ibuprofen is used to help relieve mild to moderate pain. When used with an opioid (such as morphine), it may be used to relieve moderate to severe pain. It is also used to reduce fever. Ibuprofen is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. This effect helps to decrease swelling, pain, or fever.
11-Digit NDC Billing Format:
50580023007
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 201126 - Motrin IB 200 MG Oral Tablet
  • RxCUI: 201126 - ibuprofen 200 MG Oral Tablet [Motrin]
  • RxCUI: 201126 - Motrin 200 MG Oral Tablet
  • RxCUI: 310965 - ibuprofen 200 MG Oral Tablet
  • RxCUI: 310965 - ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Johnson & Johnson Consumer 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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA077349
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-01-2016
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50580-230-011 BOTTLE in 1 CARTON / 50 TABLET, FILM COATED in 1 BOTTLE
    50580-230-021 BOTTLE in 1 CARTON / 60 TABLET, FILM COATED in 1 BOTTLE
    50580-230-031 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE
    50580-230-041 BOTTLE in 1 CARTON / 225 TABLET, FILM COATED in 1 BOTTLE
    50580-230-051 BOTTLE in 1 CARTON / 300 TABLET, FILM COATED in 1 BOTTLE
    50580-230-061 BOTTLE in 1 CARTON / 500 TABLET, FILM COATED in 1 BOTTLE
    50580-230-082 TABLET, FILM COATED in 1 POUCH
    50580-230-0950 POUCH in 1 CARTON / 2 TABLET, FILM COATED in 1 POUCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50580-230-07?

    The NDC Packaged Code 50580-230-07 is assigned to a package of 1 bottle in 1 carton / 24 tablet, film coated in 1 bottle of Motrin Ib, a human over the counter drug labeled by Johnson & Johnson Consumer Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 50580-230 included in the NDC Directory?

    Yes, Motrin Ib with product code 50580-230 is active and included in the NDC Directory. The product was first marketed by Johnson & Johnson Consumer Inc. on July 01, 2016 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 NDC billing unit for package 50580-230-07?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 50580-230-07?

    The 11-digit format is 50580023007. 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
    5-3-250580-230-075-4-250580-0230-07