Famotidine Tablet, Film Coated
Product Images NDC 72789-345

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 72789-345). 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

72789345 Label (72789345)

Label for famotidine USP 40 mg film-coated tablets by PD-Rx Pharmaceuticals, Inc. The label indicates an NDC of 72789-345-30 and a quantity of 30 tablets. Additional details include expiration date 01/2026, lot number H23B20, and usage instructions spaces. The label features text warnings and storage instructions, a barcode, and manufacturer information including location in Oklahoma City, OK.*

FDA Label Image

Famotidine-str (Famotidine Str)

Chemical structure of famotidine, showing its molecular arrangement with atoms and bonds including sulfur, nitrogen, and carbon groups typical of the active ingredient famotidine.*

* 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.