Prednisone
Product Images NDC 51655-726

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 51655-726). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Pharmaceuticals, 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 726 21 Master Bottle Label Approval Rev A 06 21)

Label (51655 726 21 Master Bottle Label Approval   Rev A 06 21)
This is a description of PredniSONE Tablets with 10 mg strength and a pack size of 21 tablets. It is a prescription-only medication, and the dosage instructions can be found in the package insert. The tablets should be stored between 20° - 25°C (68° - 77°F) in the original container and protected from moisture. The lot number is 0000000000, and it contains 10 mg of prednisone in each tablet. The tablets were repackaged by Northwind Pharmaceuticals and distributed by Hikma Pharmaceuticals USA Inc. The product is identified by its NDC code 51655-726-21 and GTIN code 00351655726211. The S/N number is 000000000000000, and the product's expiration date is 00/00/0000.*
FDA Label Image

Chem-pred.jpg (Chem Pred)

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