Famotidine Tablet, Film Coated
Product Images NDC 70000-0048

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 70000-0048). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leader/ Cardinal Health 110, 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

Package Label-principal Display Panel -10 mg (90 Tablets Container Label) (Famotidine Fig1)

Package Label-principal Display Panel -10 mg (90 Tablets Container Label) (Famotidine Fig1)
The packaging label for Famotidine Tablets 10 mg by Leader/Cardinal Health 110, Inc. It is an original strength acid reducer, with 30 film-coated tablets per bottle. The label highlights its use to prevent and relieve heartburn due to acid indigestion and includes a 100% money back guarantee. The NDC code 70000-0048-1 is visible, along with warning and directions text.*
FDA Label Image

Package Label-principal Display Panel -10 mg (30 Tablets Container Carton Label) (Famotidine Fig2)

Package Label-principal Display Panel -10 mg (30 Tablets Container Carton Label) (Famotidine Fig2)
Packaging label for Famotidine 10 mg film-coated tablets by Leader/Cardinal Health 110, Inc. The label identifies the product as an Original Strength Acid Reducer with 30 tablets per container. It includes active ingredient information, warnings, directions for use, and a comparison statement with Original Strength Pepcid AC. The label highlights the product is an acid reducer for oral administration and features a 100% money-back guarantee.*

* 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.