Prednisone Tablet
Product Images NDC 51655-701

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 Prednisone (NDC 51655-701). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 701 18 Master Bottle Label Approval Rev A 06 21)

Label (51655 701 18 Master Bottle Label Approval   Rev A 06 21)
Label for PredniSONE Tablets, USP, 20 mg, containing 18 tablets. The product is prescription only and distributed by Northwind Pharmaceuticals, Indianapolis, IN. Storage instructions recommend 20°-25°C (68°-77°F) and keeping the product out of children's reach in original container. The label includes the NDC 51655-701-18 and batch details.*
FDA Label Image

Chem-pred.jpg (Chem Pred)

Chem-pred.jpg (Chem Pred)
Chemical structure diagram of the active ingredient PredniSONE shown as a skeletal formula with labeled oxygen, hydroxyl, hydrogen, and methyl groups illustrating the molecular framework of this corticosteroid compound.*

* 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.