Prednisone Tablet
Product Images NDC 10135-777

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Prednisone (NDC 10135-777). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex Pharmaceuticals, 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

775-01 (775 01)

PredniSONE Tablets, USP 2.5 mg oral tablets packaging label by Marlex Pharmaceuticals, Inc. The label indicates a quantity of 100 tablets, Rx only. Storage instructions and usage warnings are included, along with the NDC code 10135-0775-01 and a barcode.*

FDA Label Image

776-01 (776 01)

Label for Prednisone Tablets USP, 5 mg, manufactured by Marlex Pharmaceuticals, Inc. The label indicates oral tablets for prescription use, packaged in a container of 100 tablets. Storage instructions and dosage guidelines are provided, along with a barcode and manufacturer details.*

FDA Label Image

776-10 (776 10)

Packaging label for Prednisone Tablets, USP 5 mg oral tablets by Marlex Pharmaceuticals, Inc. The label indicates 1000 tablets in the package and includes storage instructions, a barcode, and warnings to keep the medication out of reach of children. The product is prescription only.*

FDA Label Image

777-01 (777 01)

PredniSONE Tablets USP 10 mg oral tablets by Marlex Pharmaceuticals, Inc. The image shows a medication package label for a 100-tablet bottle. Label includes storage instructions to keep at 20°C to 25°C, protection from moisture, and child-resistant container use. It states Rx only and provides manufacturer details in New Castle, Delaware.*

FDA Label Image

777-10 (777 10)

Label for PredniSONE Tablets USP 10 mg by Marlex Pharmaceuticals, Inc. The label states the product is oral tablets, prescription only, with a package size of 1000 tablets. Storage and usage instructions are included along with the manufacturing details for Marlex Pharmaceuticals in New Castle, DE. The label features a barcode and NDC 10135-0777-10.*

FDA Label Image

778-01 (778 01)

Label for PredniSONE Tablets, USP 20 mg manufactured by Marlex Pharmaceuticals, Inc. The label states the product is prescription only and contains 100 oral tablets. Storage instructions include keeping the tablets at 20°C to 25°C and protecting from moisture in a child-resistant container. The NDC code is visible, and safety warnings emphasize keeping medication out of children's reach.*

FDA Label Image

778-05 (778 05)

Label of Prednisone Tablets, USP 20 mg, oral tablets, by Marlex Pharmaceuticals, Inc. The label states package contains 500 tablets. Directions mention prescription use only and storage information. Barcode and unique NDC number are visible on the right side.*

FDA Label Image

778-10 (778 10)

The label for PredniSONE Tablets, USP 20 mg, an oral prescription drug by Marlex Pharmaceuticals, Inc. The package contains 1000 tablets. The label includes dosage instructions, storage conditions at 20°C to 25°C, moisture protection, and child-resistant packaging information. A barcode and the NDC number 10135-0778-10 are visible.*

FDA Label Image

779-01 (779 01)

Packaging label for PredniSONE Tablets, USP 50 mg by Marlex Pharmaceuticals, Inc. The label indicates 100 tablets per container. It includes usage and storage instructions, caution to keep out of reach of children, and states 'Rx Only'. The label features barcodes and batch information.*

FDA Label Image

Structure (Prednisone Structure)

Chemical structure of the active ingredient prednisone showing its steroid backbone with ketone and hydroxyl functional groups.*

* 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.