NDC Package 63868-480-50 Ranitidine

Tablet, 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:
63868-480-50
Package Description:
1 BOTTLE in 1 CARTON / 50 TABLET, COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Ranitidine
Non-Proprietary Name:
Ranitidine
Substance Name:
Ranitidine Hydrochloride
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:
63868048050
NDC to RxNorm Crosswalk:
  • RxCUI: 198191 - ranitidine 150 MG Oral Tablet
  • RxCUI: 198191 - ranitidine 150 MG (as ranitidine HCl 168 MG) Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Chain Drug Marketing Association
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA078192
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-01-2018
    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
    63868-480-241 BOTTLE in 1 CARTON / 24 TABLET, COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63868-480-50?

    The NDC Packaged Code 63868-480-50 is assigned to a package of 1 bottle in 1 carton / 50 tablet, coated in 1 bottle of Ranitidine, a human over the counter drug labeled by Chain Drug Marketing Association. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 63868-480 included in the NDC Directory?

    Yes, Ranitidine with product code 63868-480 is active and included in the NDC Directory. The product was first marketed by Chain Drug Marketing Association on July 01, 2018 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 63868-480-50?

    The 11-digit format is 63868048050. 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
    5-3-263868-480-505-4-263868-0480-50