Prednisolone Sodium Phosphate Solution
Product Images NDC 0121-0777

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 Prednisolone Sodium Phosphate (NDC 0121-0777). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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 (Prednisolone 1)

FDA Label Image

Principal Display Panel (237 mL bottle label)

Principal Display Panel (237 mL bottle label)
This is a description for Prednisolone Sodium Phosphate Oral Solution, a medication that is equivalent to prednisone. The medication should be stored in a refrigerated space, in a tight, light-resistant glass or PET plastic container as defined by USP, and it should be kept out of reach of children. It is alcohol-free and dye-free and is only available with a prescription. The medication is made by Pharmaceutical Associates, Inc. and is a palatable solution that contains 20 mg of prednisolone base per 5 mL (teaspoonful). For complete dosage information, a person should consult the package insert.*

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