Famotidine Powder, For Suspension
Product Images NDC 67877-775

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 67877-775). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Laboratories, Llc, 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

Fam01 (Fam01)

Chemical structure diagram of famotidine, showing its molecular arrangement with labeled atoms and bonds corresponding to the drug's chemical formula.*

FDA Label Image

Fam02-1a (Fam02 1a)

The label for Famotidine for Oral Suspension, USP, strength 40 mg/5 mL, provides directions for constitution, storage instructions, and dosage details. It includes the proprietary name Famotidine, the dosage form powder for suspension, a volume indication of 50 mL when reconstituted, and the statement "FOR ORAL USE ONLY". The label features the Ascend Laboratories logo and includes an NDC number 67877-775-89, with a barcode and manufacturer 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.