Mycophenolic Acid Tablet, Delayed Release
Product Images NDC 70436-173

View Photos of 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 Mycophenolic Acid (NDC 70436-173). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Slate Run 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

Chemical Structure (Chemical Structure)

Chemical Structure (Chemical Structure)
Chemical structure of mycophenolic acid showing its molecular framework with rings and functional groups, including a sodium salt moiety, illustrated in a standard 2D line representation.*
FDA Label Image

180 mg, 120 Counts (Mycophenolic Acid 180mg 120ct)

180 mg, 120 Counts (Mycophenolic Acid 180mg 120ct)
Label for Mycophenolic Acid Delayed-Release Tablets, USP 180 mg by Slate Run Pharmaceuticals, LLC. The label shows NDC 70436-172-23 and indicates the package contains 120 tablets. It includes storage instructions, manufacturer information, and a barcode. The label specifies the delayed-release tablet contains mycophenolate sodium equivalent to 180 mg mycophenolic acid.*
FDA Label Image

360 mg, 120 Counts (Mycophenolic Acid 360mg 120ct)

360 mg, 120 Counts (Mycophenolic Acid 360mg 120ct)
Mycophenolic Acid Delayed-Release Tablets, USP 360 mg oral tablets, packaged in a bottle of 120. Label shows that each delayed-release tablet contains mycophenolate sodium equivalent to 360 mg mycophenolic acid. Manufactured by Yichang Humanwell in China and distributed by Slate Run Pharmaceuticals, LLC. The package is child-resistant with storage instructions at 20° to 25°C.*

* 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.