Sucralfate Suspension
Product Images NDC 0378-9205

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 Sucralfate (NDC 0378-9205). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan 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

Sucralfate Structural Formula (Image 01)

FDA Label Image

Sucralfate Oral Suspension 1 G/10 mL Label (Image 02)

Sucralfate Oral Suspension 1 G/10 mL Label (Image 02)
This is a description of an oral suspension medication called Sucralfate. The bottle contains 9205-35 NDC number and can hold up to 20mL of the suspension. The medication is intended for oral administration only and should be shaken well before use. It should also not be frozen. Each 10 mL of the suspension contains 1 USP Sucralfate. The recommended adult dosage is 2 teaspoons four times a day, on an empty stomach, as per the accompanying prescribing information. The medication should be stored at controlled room temperature (20° to 25°C or 68°F to 77°F). The description also includes warning information to keep the medication safely out of reach of children.*

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