Famotidine Tablet, Film Coated
Product Images NDC 55319-057

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 55319-057). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Family Dollar Stores, Llc, 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

Package Label-principal Display Panel -20 mg (25 Tablets, Container Label) (Famotidine 20mg Fig1)

Package Label-principal Display Panel -20 mg (25 Tablets, Container Label) (Famotidine 20mg Fig1)
Packaging label for Famotidine maximum strength tablets, USP 20 mg, oral film-coated tablets. The label indicates 25 tablets per bottle, marketed as an acid reducer to prevent and relieve heartburn due to acid indigestion. The labeler is Family Dollar Stores, LLC, with NDC 55319-057-25. The label also includes warnings, directions, and storage information.*
FDA Label Image

Package Label-principal Display Panel -20 mg (50 Tablets, Container Carton Label) (Famotidine 20mg Fig2)

Package Label-principal Display Panel -20 mg (50 Tablets, Container Carton Label) (Famotidine 20mg Fig2)
Family Wellness Maximum Strength Famotidine 20 mg film-coated tablets carton. The label highlights the product as an acid reducer with 25 tablets per package. It includes drug facts, active ingredient Famotidine USP 20 mg, usage instructions, warnings, inactive ingredients, and contact information. Distributed by Midwood Brands, LLC and labeled for Family Dollar Stores, LLC.*

* 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.