Famotidine Tablet, Film Coated
Product Images NDC 72789-453

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 72789-453). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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

72789453 Label (72789453)

72789453 Label (72789453)
Label for FAMOTIDINE USP 40 MG film-coated tablets, containing 30 tablets per bottle. The label shows the NDC code 72789-453-30 and identifies PD-Rx Pharmaceuticals, Inc. as the labeler in Oklahoma City, OK. The lot number is K24C46 with an expiration date of 01/2027. The label includes dosing instructions spaces, a warning to keep out of reach of children, and a QR code.*
FDA Label Image

Famotidine-str (Famotidine Str)

Famotidine-str (Famotidine Str)
Chemical structure of famotidine showing the arrangement of atoms including nitrogen, sulfur, carbon, and oxygen in the molecular framework.*

* 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.