Prednisolone Sodium Phosphate Solution
Product Images NDC 62135-330

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Prednisolone Sodium Phosphate (NDC 62135-330). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, 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

Prednisolone Sodium Phosphate Oral Solution 01

Chemical structure of prednisolone sodium phosphate, showing its steroid backbone with characteristic hydroxyl, carbonyl, and phosphate groups, consistent with its identity as the active ingredient in Prednisolone Sodium Phosphate oral solution.*

FDA Label Image

Prednisolone Sodium Phosphate Oral Solution 02

Prednisolone Sodium Phosphate Oral Solution 5 mg/5 mL label by Chartwell RX, LLC. The label states the product is alcohol, dye, and sugar free, intended for oral use with a package size of 120 mL (4 fluid ounces). It includes dosage and storage information, the NDC 62135-330-41, and a barcode. The label is white with blue accents and features a U.S. flag indicating it is made in the USA.*

* 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.