NDC 67091-241 Famotidine - Acid Controller

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
67091-241
Proprietary Name:
Famotidine - Acid Controller
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Winco Foods, Llc
Labeler Code:
67091
Start Marketing Date: [9]
05-01-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
8 MM
Imprint(s):
035
036
Score:
1

Product Packages

NDC Code 67091-241-25

Package Description: 25 TABLET, FILM COATED in 1 BOTTLE

Product Details

What is NDC 67091-241?

The NDC code 67091-241 is assigned by the FDA to the product Famotidine - Acid Controller which is product labeled by Winco Foods, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67091-241-25 25 tablet, film coated in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Famotidine - Acid Controller?

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

Which are Famotidine - Acid Controller UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Famotidine - Acid Controller Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Famotidine - Acid Controller?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".