Image 1
Chemical structure of Famotidine showing the arrangement of atoms including nitrogen, sulfur, carbon, and sulfur dioxide amine functional groups.*
Famotidine Tablet, Film Coated
Product Images NDC 0172-5728
3 FDA label images from Teva Pharmaceuticals Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 0172-5728). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Teva Pharmaceuticals Usa, 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.
Image 2
Famotidine Tablets USP 20 mg film-coated oral tablets label by Teva Pharmaceuticals USA, Inc. The label includes the NDC number 0172-5728-60, package count of 100 tablets, barcode, and storage and disposal information. The design features blue and black text on a white background with the Teva logo in blue.*
Image 3
Famotidine Tablets USP 40 mg film-coated oral tablets label by Teva Pharmaceuticals USA, Inc. The label shows the NDC number 0172-5729-60 and states the package contains 100 tablets. It includes dosing and storage instructions, safety warnings, and a non-varnish area for lot and expiration 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.
