Prednisone
Product Images NDC 59746-175

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Prednisone (NDC 59746-175). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jubilant Cadista Pharmacuticals Inc., 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 (59746 172 06)

Label for Prednisone Tablets USP, 5 mg, manufactured by Jubilant Cadista Pharmaceuticals Inc. The label indicates a package size of 100 tablets, with instructions to dispense in a tight, light-resistant container, and storage at 20-25°C (68-77°F). It also notes that the product is Rx only and includes an NDC number 59746-172-06.*

FDA Label Image

Label (59746 173 06)

Label for PredniSONE Tablets, USP 10 mg by Jubilant Cadista Pharmaceuticals Inc. The label includes instructions to see the package insert for complete information, storage recommendations at 20-25°C, and notes to dispense in a tight, light-resistant container and keep the patient under close observation. The package contains 100 tablets marked Rx Only.*

FDA Label Image

Label (59746 175 06)

Prednisone 20 mg Tablets, USP label by Jubilant Cadista Pharmaceuticals Inc. The label shows a white background with black and orange text, includes the dosage strength (20 mg), quantity (100 tablets), and a note that the product is prescription only. Storage and dispensing instructions are present along with the NDC number 59746-175-06 and barcode.*

FDA Label Image

Image (Prednisone Tablet 01)

Chemical structure diagram of Prednisone showing its steroid backbone with various functional groups including hydroxyl, keto, and methyl groups as depicted in the molecular formula.*

* 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.