Famotidine Powder, For Suspension
Product Images NDC 72162-2599

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 72162-2599). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Chemstructure (Chemstructure)

Chemical structure diagram showing the molecular structure of famotidine, the active ingredient in the product. The diagram depicts the arrangement of atoms and bonds characteristic of famotidine's chemical composition.*

FDA Label Image

Label (Lbl721622599)

Label for Famotidine for Oral Suspension USP powder for suspension, 40 mg/5 mL strength. The label indicates a 50 mL bottle size when reconstituted. It is relabeled by Bryant Ranch Prepack, Inc., and manufactured by Carnegie Pharmaceuticals LLC. Directions and storage instructions for reconstitution and use are also included.*

* 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.