Famotidine Powder, For Suspension
Product Images NDC 72162-2599

View Photos of Packaging, Regulatory Labels, and Product Appearance

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)

FDA Label Image

Label (Lbl721622599)

Label (Lbl721622599)
This text provides information on a medication containing 400 mg of Famotidine in each bottle. When reconstituted, each teaspoonful (5mL) contains 40 mg of Famotidine. The suspension should be protected from freezing and discarded after 30 days. Inactive ingredients include anhydrous citric acid, powdered cellulose, sucrose, xanthan gum, and banana, cherry, and mint flavor. Methylparaben sodium, propylparaben sodium, and sodium benzoate are used as preservatives. The adult dosage information can be accessed by scanning the package insert QR code. It notes that the bottle is oversized for shaking before use. Directions for reconstitution involve adding 46 mL of water to the bottle and shaking well. The medication should be stored at controlled room temperature.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.