Prednisolone Sodium Phosphate Oral Solution
Product Images NDC 44523-182

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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)

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)

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