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  5. NDC Package Code: 49348-473-44 Ranitidine

NDC Package 49348-473-44 Ranitidine

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
49348-473-44
Package Description:
1 BOTTLE in 1 CARTON / 30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
49348-473
Proprietary Name:
Ranitidine
Usage Information:
Adults and children 12 years and over: to relieve symptoms, swallow 1 tablet with a glass of waterto prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburncan be used up to twice daily (do not take more than 2 tablets in 24 hours)children under 12 years: ask a doctor
11-Digit NDC Billing Format:
49348047344
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: 312773 - ranitidine 75 MG Oral Tablet
  • RxCUI: 312773 - ranitidine 75 MG (as ranitidine hydrochloride 84 MG) Oral Tablet
    • Labeler Name:
    Sunmark
    Sample Package:
    No
    Start Marketing Date:
    09-20-2013
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I
    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
    49348-473-121 BOTTLE in 1 CARTON / 60 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 49348-473-44?

    The NDC Packaged Code 49348-473-44 is assigned to a package of 1 bottle in 1 carton / 30 tablet, film coated in 1 bottle of Ranitidine, labeled by Sunmark. The product's dosage form is and is administered via form.

    Is NDC 49348-473 included in the NDC Directory?

    No, Ranitidine with product code 49348-473 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Sunmark on September 20, 2013 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 49348-473-44?

    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 49348-473-44?

    The 11-digit format is 49348047344. 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
    5-3-249348-473-445-4-249348-0473-44