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  5. NDC Package Code: 51660-036-26 Famotidine - Acid Controller

NDC Package 51660-036-26 Famotidine - Acid Controller

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
51660-036-26
Package Description:
25 TABLET, FILM COATED in 1 BOTTLE
Product Code:
51660-036
Proprietary Name:
Famotidine - Acid Controller
Usage Information:
•adults and children 12 years and over: •to relieve symptoms, swallow 1 tablet with a glass of water. Do not chew.•to prevent symptoms, swallow 1 tablet with a glass of water at any time from 10 to 60 minutes before eating food or drinking beverages that cause heartburn•do not use more than 2 tablets in 24 hours•children under 12 years: ask a doctor
11-Digit NDC Billing Format:
51660003626
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
25 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 310273 - famotidine 20 MG Oral Tablet
    • Labeler Name:
    Ohm Laboratories Inc.
    Sample Package:
    No
    Start Marketing Date:
    05-31-2017
    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.

    Frequently Asked Questions

    What is NDC 51660-036-26?

    The NDC Packaged Code 51660-036-26 is assigned to a package of 25 tablet, film coated in 1 bottle of Famotidine - Acid Controller, labeled by Ohm Laboratories Inc.. The product's dosage form is and is administered via form.

    Is NDC 51660-036 included in the NDC Directory?

    No, Famotidine - Acid Controller with product code 51660-036 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Ohm Laboratories Inc. on May 31, 2017 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 51660-036-26?

    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 25.

    What is the 11-digit format for NDC 51660-036-26?

    The 11-digit format is 51660003626. 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
    5-3-251660-036-265-4-251660-0036-26