NDC Package 49348-873-59 Sunmark Ibuprofen Pm

Diphenhydramine Citrate And 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:
49348-873-59
Package Description:
1 BOTTLE in 1 CARTON / 40 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Sunmark Ibuprofen Pm
Non-Proprietary Name:
Diphenhydramine Citrate And Ibuprofen
Substance Name:
Diphenhydramine Citrate; Ibuprofen
Usage Information:
•do not take more than directed •adults and children 12 years and over: take 2 caplets at bedtime•do not take more than 2 caplets in 24 hours
11-Digit NDC Billing Format:
49348087359
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: 895664 - ibuprofen 200 MG / diphenhydrAMINE citrate 38 MG Oral Tablet
  • RxCUI: 895664 - diphenhydramine citrate 38 MG / ibuprofen 200 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Strategic Sourcing Services Llc
    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:
    ANDA079113
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-18-2009
    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 49348-873-59?

    The NDC Packaged Code 49348-873-59 is assigned to a package of 1 bottle in 1 carton / 40 tablet, film coated in 1 bottle of Sunmark Ibuprofen Pm, a human over the counter drug labeled by Strategic Sourcing Services Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 49348-873 included in the NDC Directory?

    Yes, Sunmark Ibuprofen Pm with product code 49348-873 is active and included in the NDC Directory. The product was first marketed by Strategic Sourcing Services Llc on February 18, 2009 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 NDC billing unit for package 49348-873-59?

    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 49348-873-59?

    The 11-digit format is 49348087359. 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
    5-3-249348-873-595-4-249348-0873-59