Prednisone Tablet
Product Images NDC 59651-484

3 FDA label images from Aurobindo Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Prednisone (NDC 59651-484). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (1 mg (100 Tablet Bottle))

Package Label-principal Display Panel (1 mg (100 Tablet Bottle))
Label for Prednisone Tablets, USP 1 mg by Aurobindo Pharma Limited. The label states 100 tablets per container and includes storage instructions, color additive information, and manufacturer details showing distribution by Aurobindo Pharma USA, Inc. The label features dosage form, strength, and NDC 59651-484-01.*
FDA Label Image

Package Label-principal Display Panel (1 mg 100(10x10) Unit-dose Tablets)

Package Label-principal Display Panel (1 mg 100(10x10) Unit-dose Tablets)
Packaging label for predniSONE Tablets, USP 1 mg by Aurobindo Pharma Limited. The label shows the tablets are oral, unit-dose, with a total count of 100 (10x10). It includes NDC 59651-484-78 and instructions to store at 20° to 25°C, protect from moisture, and refers to the package insert for complete prescribing information. Distributed by Aurobindo Pharma USA, Inc.*
FDA Label Image

Chemical Structure (Prednisone Str)

Chemical Structure (Prednisone Str)
Chemical structure diagram of prednisone, showing its steroid nucleus and functional groups, consistent with its identification as the active ingredient in the PREDNISONE 1 mg oral tablet by Aurobindo Pharma Limited.*

* 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.