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)
This is a description of PredniSONE Tablets, USP, 5mg with 21 tablets in a container. It has a National Drug Code (NDC) of 51655-765-21 and is Rx only. Patients should refer to the package insert for dosage instructions and store the container at controlled room temperature (20° - 25°C). Each tablet contains Prednisone, USP 5mg. The container must be kept out of reach from children, protected from light and moisture, and tightly closed. The medication is repackaged by Northwind Pharmaceuticals in Indianapolis, IN and has a GTIN and S/N of 000000000000000. It expires on 00/00/0000 with a lot number of 0000000000.*
FDA Label Image

Structural Formula (Prednisone Tablets Usp 01)

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