Mycophenolic Acid Tablet, Delayed Release
Product Images NDC 0904-6785

3 FDA label images from Major Pharmaceuticals · 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 0904-6785). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

Be154e5a 0753 Bb76 B9a6 Ee5d4b6492b5 00

Be154e5a 0753 Bb76 B9a6 Ee5d4b6492b5 00
Label for Mycophenolic Acid delayed release tablets from Major Pharmaceuticals. The label indicates a 360 mg strength in oral tablet form, packaged as unit dose with 100 tablets. The label includes dosing instructions, storage conditions, and a note to dispense with a medication guide. NDC codes 0904-6786-61 and 0904-6786-61 are shown.*
FDA Label Image

Be154e5a 0753 Bb76 B9a6 Ee5d4b6492b5 01

Be154e5a 0753 Bb76 B9a6 Ee5d4b6492b5 01
Packaging label for Major Pharmaceuticals Mycophenolic Acid delayed release tablets USP, 180 mg strength. The label displays the product name, strength, dosage form as delayed release tablets, unit dose packaging, and the labeler Major Pharmaceuticals. It includes directions to dispense with medication guide and states Rx only with a package count of 30 tablets.*
FDA Label Image

Mycophenolic-structure (Mycophenolicfigure)

Mycophenolic-structure (Mycophenolicfigure)
Chemical structure of mycophenolic acid sodium salt, depicting its molecular connectivity with specific functional groups including aromatic rings, hydroxyl group, and carboxylate linked to a sodium ion. The structure corresponds to the active ingredient mycophenolic acid.*

* 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.