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  5. NDC Package Code: 67091-241-25 Famotidine - Acid Controller

NDC Package 67091-241-25 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:
67091-241-25
Package Description:
25 TABLET, FILM COATED in 1 BOTTLE
Product Code:
67091-241
Proprietary Name:
Famotidine - Acid Controller
Usage Information:
Famotidine USP, 10 mg•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 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 doctorFamotidine USP, 20 mg•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:
67091024125
NDC to RxNorm Crosswalk:
  • RxCUI: 199047 - famotidine 10 MG Oral Tablet
  • RxCUI: 310273 - famotidine 20 MG Oral Tablet
    • Labeler Name:
    Winco Foods, Llc
    Sample Package:
    No
    Start Marketing Date:
    05-01-2012
    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 67091-241-25?

    The NDC Packaged Code 67091-241-25 is assigned to a package of 25 tablet, film coated in 1 bottle of Famotidine - Acid Controller, labeled by Winco Foods, Llc. The product's dosage form is and is administered via form.

    Is NDC 67091-241 included in the NDC Directory?

    No, Famotidine - Acid Controller with product code 67091-241 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Winco Foods, Llc on May 01, 2012 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 11-digit format for NDC 67091-241-25?

    The 11-digit format is 67091024125. 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
    5-3-267091-241-255-4-267091-0241-25