Prednisolone Sodium Phosphate Oral Solution
Product Images NDC 44523-182

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Prednisolone Sodium Phosphate Oral Solution (NDC 44523-182). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Biocomp Pharma, 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

Prednisolone Sodium Phosphate Oral Solution 25 mg/5 mL Label Ndc: 44523-182-08 (Bcp 11424 L182c080619 Prednisolone Sodium Phosphate Oral Solution 25mg 5ml Label)

This is a medication description. The medication has NDC number 44523-182-08 and is a phosphate oral solution that is equivalent to prednisolone. The dosage information is available on the package insert. The solution is palatable, and it comes in 25 mg/5 mL tight, light-resistant glass or PET plastic containers as defined in the USP. The solution should be refrigerated and kept highly closed between 2° to 8°C (36° to 46°F), and away from children. This medication is alcohol-free and dye-free, and it is manufactured by BioComp Pharma Inc. in San Antonio, TX. The bottle has a capacity of 8 fl oz (237 mL).*

FDA Label Image

Structure (Structure)

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.