Structural Formula (Famotidine For Oral Suspension Usp 1)
Famotidine Powder, For Suspension
Product Images NDC 69238-2090
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Product Visual Gallery
This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 69238-2090). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Amneal Pharmaceuticals Ny 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.
Product Images & Figures Index
Label (Famotidine For Oral Suspension Usp 2)
This is a prescribing information label for Famotidine, a medication used for acid reflux and heartburn. It provides instructions for reconstitution of the dry powder and suspension, dosage, storage requirements, and expiration date. When reconstituted, each teaspoonful (5ml) contains 40mg of famotidine, USP. It is suitable for oral use and should be shaken before use. The label is produced by Amneal Pharmaceuticals LLC and distributed in Bridgewater, NJ, USA.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
