Famotidine Tablet, Film Coated
Product Images NDC 83324-003

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 83324-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chain Drug Marketing Association, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Amotidinetablets10mg30scountcarton (Famotidinetablets10mg30scountcarton)

Famotidine Tablets USP 10 mg, film-coated oral tablets by Chain Drug Marketing Association, Inc. The label indicates 30 tablets per package under the brand Quality Choice Original Strength. The packaging highlights famotidine as an acid reducer to prevent and relieve heartburn due to acid indigestion from food and beverages.*

FDA Label Image

Famotidinetablets10mg30scountcontainer (Famotidinetablets10mg30scountcontainer)

Packaging label for famotidine tablets USP, 10 mg, film-coated oral tablets. The label features the brand Quality Choice and states it is an acid reducer for heartburn relief. The carton contains 30 tablets, distributed by CDMA, Inc. The label includes active ingredient, purpose, warnings, uses, directions for use, and batch coding details area with barcode.*

FDA Label Image

Famotidinetablets20mg50scountcarton (Famotidinetablets20mg50scountcarton)

Label for Famotidine Tablets USP, 20 mg, film-coated oral tablets by CHAIN DRUG MARKETING ASSOCIATION, INC. The label indicates 50 tablets per bottle and highlights the product as an acid reducer to prevent and relieve heartburn due to acid indigestion. It includes Drug Facts, directions, warnings, inactive ingredients, and manufacturer details.*

FDA Label Image

Famotidinetablets20mg50scountcontainer (Famotidinetablets20mg50scountcontainer)

Label for famotidine tablets USP, 20 mg, film-coated oral tablets. The label indicates the product is an acid reducer with a quantity of 50 tablets. It is distributed by Chain Drug Marketing Association, Inc. The front label includes a barcode, satisfaction guarantee logo, and a varnish area for batch coding. The back label and second layer contain detailed drug facts including active ingredient, uses, warnings, and directions for adults and children 12 years and over.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.