Prednisolone Sodium Phosphate Solution
Product Images NDC 17856-0815

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Prednisolone Sodium Phosphate (NDC 17856-0815). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

Image 1 (17856 0815 01 Case Label)

Image 1 (17856 0815 01 Case Label)
Prednisolone Sodium Phosphate Oral Solution 15 mg/5 mL label by Atlantic Biologicals Corp. The label indicates the dosage strength, packaging instructions to dispense in a light-resistant container, storage temperature, and child safety warning. It includes barcode, QR code, expiration date 01/13/25, quantity of 72 cups and reordering information.*
FDA Label Image

Image 2 (17856 0815 02 Case Label)

Image 2 (17856 0815 02 Case Label)
Label for Prednisolone Sodium Phosphate oral solution, 15 mg per 5 mL, delivering 30 mg per 10 mL, from Atlantic Biologicals Corp. The label notes the product is alcohol/dye free and should be stored at 20°-25°C in a tight, light-resistant glass or PET container. The package contains 72 cups of solution.*
FDA Label Image

Image 3 (17856 0815 03 Case Label)

Image 3 (17856 0815 03 Case Label)
Label for Prednisolone Sodium Phosphate Oral Solution, 15 mg per 5 mL, in a dosage form delivered via syringes. The label indicates 48 syringes per package, manufactured by Atlantic Biologicals Corp., Miami, FL. It specifies storage instructions, alcohol/dye-free formulation, and includes a barcode and expiration details.*
FDA Label Image

Image 4 (17856 0815 03 Rev. 1 Label)

Image 4 (17856 0815 03 Rev. 1 Label)
Label for Prednisolone Sodium Phosphate oral solution 15 mg/5 mL. The label states the product is prescription only, alcohol and dye free, distributed by Atlantic Biologicals Corp., with space for expiration date and lot number. Includes a barcode and product revision number.*
FDA Label Image

Structure (Pred Structure)

Structure (Pred Structure)
Chemical structure diagram of prednisolone sodium phosphate showing its molecular arrangement with hydroxyl groups, phosphate group, and steroid nucleus.*

* 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.