Prednisone Tablet
Product Images NDC 70518-3401

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Prednisone (NDC 70518-3401). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Structure (6ed4f90c 6fcc 4389 935f 72851f3ffb0c 01)

FDA Label Image

Remedy_label (Remedy Label)

This is a medication called predniSONE, in tablet form, with a strength of 20 mg. The NDC number is 70518-3401-00 and it was manufactured by Strides Pharma Inc. in East Brunswick, NJ. The lot number and expiration date are not available. The medication should be kept out of children's reach and directions for use should be followed as per package insert. It should be stored at room temperature between 15-30°C (59-86°F) and is available for prescription only. It has been repackaged by RemedyRepack Inc. in Indiana, PA.*

FDA Label Image

Mm2 (Prednisone 20mg 70518 3401 01)

Description: This is a medication called predniSONE in tablet form with a strength of 20mg. The National Drug Code (NDC) number is 70518-3401-01 and it was manufactured by Strides Pharma Inc. in East Brunswick, NJ. The medication comes in a bottle with a quantity of 13 tablets and should be kept out of reach of children. There is a lot number and expiration date provided, and the medication should be stored between 25° and 30°C (59-86°F). Directions for use are included in the package insert. This medication is only available with a prescription and has been repackaged by RemedyRepack Inc. in Indiana, PA.*

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