Sucralfate Suspension
Product Images NDC 65162-062

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sucralfate (NDC 65162-062). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

Chemical Structure (Sucralfate Oral Suspension 1)

FDA Label Image

1 (Sucralfate Oral Suspension 2)

1 (Sucralfate Oral Suspension 2)
Sucralfate Oral Suspension is a medication containing 1g of sucralfate, USP per 10 mL (2 teaspoons) for oral administration only. It is recommended for adults to take 1g four times per day on an empty stomach. The medication comes in a 420 mL bottle and should be stored between 20°C to 25°C (68°F to 77°F). It is important to shake well before using and avoid freezing. There is a warning to keep this medication out of reach of children. Please refer to the package insert for full prescribing information.*
FDA Label Image

Sucralfate Oral Suspension 3

Sucralfate Oral Suspension 3
This is a description of a medication called "Sucralfate Oral Suspension" distributed by Amneal Pharmaceuticals. Each bottle contains 19/10 mL and has a National Drug Code (NDC) of 65162-062-47. The medication is available by prescription only, and the label instructs users to shake well before use and store it at 20-25°C (68-77°F). The distributed location is in Bridgewater, NJ 08807, and the prescription was revised in April 2020.*

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