Famotidine Powder, For Suspension
Product Images NDC 0527-5190

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 0527-5190). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Structural Formula (Famotidine For Oral Suspension Usp 1)

Chemical structure of famotidine showing its molecular formula with various atoms including nitrogen, sulfur, and carbon arranged in a heterocyclic ring and side chains.*

FDA Label Image

Bottle Label (Famotidine For Oral Suspension Usp 2)

Label for Famotidine for Oral Suspension, USP 40 mg/5 mL powder for suspension by Lannett Company, Inc. The label includes directions for constitution by adding purified water, storage instructions, and warnings. The container size is 55 mL when reconstituted, with a note to shake well before using. The label features the NDC number 0527-5190.*

* 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.