Prednisone Tablet
Product Images NDC 51655-765

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 51655-765). 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 765 21 Master Bottle Label Approval Rev A 07 21)

Label (51655 765 21 Master Bottle Label Approval   Rev A 07 21)
Label for PredniSONE Tablets, USP 5 mg. The package contains 21 tablets for oral use. It is a prescription-only medication labeled by Northwind Health Company, LLC, with storage instructions to keep at 20°-25°C (68°-77°F), protected from light and moisture, and out of reach of children. Additional text includes repackaging and packaging details along with lot and expiration information.*
FDA Label Image

Structural Formula (Prednisone Tablets Usp 01)

Structural Formula (Prednisone Tablets Usp 01)
Chemical structure of the active ingredient prednisone, showing its steroid backbone with hydroxyl, carbonyl, and methyl groups as part of its molecular configuration.*

* 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.