Famotidine Tablet, Film Coated
Product Images NDC 46122-737

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 46122-737). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amerisource Bergen, 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 (50 Tablets, Container Label) (Famotidine 20mg Fig1)

Package Label-principal Display Panel -20 mg (50 Tablets, Container Label) (Famotidine 20mg Fig1)
Label for Famotidine Tablets USP 20 mg film-coated tablets by Amerisource Bergen. Marketed as an acid reducer with maximum strength, the label highlights that one tablet prevents and relieves heartburn and acid indigestion. The package contains 25 tablets. The label also includes warnings, directions, storage information, and the manufacturer details including the address in Pennsylvania and a website.*
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)
Box packaging for Famotidine Tablets USP 20 mg, labeled as Acid Reducer Maximum Strength, containing 25 film-coated oral tablets. The product is an over-the-counter human drug by AmerisourceBergen under the Good Neighbor Pharmacy brand. The label includes drug facts, usage warnings, tips for managing heartburn, and a barcode.*

* 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.