Famotidine Tablet, Film Coated
Product Images NDC 69256-002

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 69256-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Harris Teeter, 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 -10 mg (30 Tablets Container Label) (Famotidine Fig1)

Package Label-principal Display Panel -10 mg (30 Tablets Container Label) (Famotidine Fig1)
Famotidine 10 mg Acid Reducer tablets, film-coated, oral dosage form, marketed by Harris Teeter, LLC. The label is blue and white with a Harris Teeter logo and states 30 tablets per bottle. It highlights the product as an original strength acid reducer that prevents and relieves heartburn due to acid indigestion. The label includes active ingredient, warnings, directions, and storage instructions.*
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)
Famotidine 10 mg Original Strength acid reducer film-coated tablets, 30 count, in a carton labeled with Harris Teeter branding. The packaging highlights use for prevention and relief of heartburn, includes usage warnings, drug facts, active ingredient, directions, and other product information. Manufactured for Harris Teeter, 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.