Famotidine Tablet, Film Coated
Product Images NDC 72036-026

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 72036-026). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Harris Teeter, 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)
Famotidine 20 mg film-coated tablets acid reducer packaging label from Harris Teeter. The label displays the brand name and strength prominently with claims to prevent and relieve heartburn due to acid indigestion. It states there are 25 tablets in the package and includes detailed usage warnings, directions, ingredients, and distributor information. The label instructs not to use if the printed foil seal is broken or missing and includes storage and lot details.*
FDA Label Image

Package Label-principal Display Panel -20 mg (25 Tablets, Container Carton Label) (Famotidine 20mg Fig2)

Package Label-principal Display Panel -20 mg (25 Tablets, Container Carton Label) (Famotidine 20mg Fig2)
Packaging label for Famotidine 20 mg film-coated tablets by Harris Teeter. The label features maximum strength acid reducer branding, with 25 tablets per package. It displays drug facts, uses, warnings, inactive ingredients, and directions for use. The label also includes a barcode and Harris Teeter branding with contact information.*

* 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.