Famotidine Powder, For Suspension
Product Images NDC 70954-316

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 70954-316). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani Pharmaceuticals, 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

Label (Famotidine Label)

This is a medication called Famotidine, available in both dry powder and suspension form. The usual adult dosage is not provided, and instructions on how to reconstitute the medication with water are given. When reconstituted, each 5 mL teaspoonful contains 40 mg of Famotidine. The medication should be stored at room temperature, and protected from light and freezing. The excess size of the bottle allows for shaking when reconstituted. The medication cannot be used beyond 30 days after being reconstituted. The manufacturer is Novitium Pharma LLC, and the medication is for oral use only. The prescription information and the expiry date are provided.*

FDA Label Image

Structure (Famotidine Structure)

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