NDC Package 11822-0500-1 Acid Reducer Plus Antacid

Famotidine,Calcium Carbonate And Magnesium Hydroxide Tablet, Chewable 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:
11822-0500-1
Package Description:
25 TABLET, CHEWABLE in 1 BOTTLE
Product Code:
Proprietary Name:
Acid Reducer Plus Antacid
Non-Proprietary Name:
Famotidine, Calcium Carbonate And Magnesium Hydroxide
Substance Name:
Calcium Carbonate; Famotidine; Magnesium Hydroxide
Usage Information:
•adults and children 12 years and over:•do not swallow tablet whole: chew completely•to relieve symptoms, chew 1 tablet before swallowing•do not use more than 2 chewable tablets in 24 hours•children under 12 years: ask a doctor
11-Digit NDC Billing Format:
11822050001
NDC to RxNorm Crosswalk:
  • RxCUI: 283641 - famotidine 10 MG / calcium carbonate 800 MG / magnesium hydroxide 165 MG Chewable Tablet
  • RxCUI: 283641 - calcium carbonate 800 MG / famotidine 10 MG / magnesium hydroxide 165 MG Chewable Tablet
  • RxCUI: 283641 - calcium carbonate 800 MG / famotidine 10 MG / milk of magnesia 165 MG Chewable Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Rite Aid Corporation
    Dosage Form:
    Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA077355
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-08-2013
    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
    11822-0500-250 TABLET, CHEWABLE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 11822-0500-1?

    The NDC Packaged Code 11822-0500-1 is assigned to a package of 25 tablet, chewable in 1 bottle of Acid Reducer Plus Antacid, a human over the counter drug labeled by Rite Aid Corporation. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 11822-0500 included in the NDC Directory?

    Yes, Acid Reducer Plus Antacid with product code 11822-0500 is active and included in the NDC Directory. The product was first marketed by Rite Aid Corporation on November 08, 2013 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 11822-0500-1?

    The 11-digit format is 11822050001. 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 5-4-1 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
    5-4-111822-0500-15-4-211822-0500-01