Myfortic Tablet, Delayed Release
Product Images NDC 0078-0386

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 Myfortic (NDC 0078-0386). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novartis Pharmaceuticals Corporation, 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

Mycophenolic Acid Structural Formula. (Myfortic 01)

Mycophenolic Acid Structural Formula. (Myfortic 01)
Chemical structure of mycophenolic acid, the active ingredient in Myfortic tablets. The diagram shows the molecular arrangement including hydroxyl, methoxy, and carboxylate groups with a sodium ion.*
FDA Label Image

Principal Display Panelpackage Label – 180 mgrx Only Ndc 0078-0385-66 (Myfortic 02)

Principal Display Panelpackage Label – 180 mgrx Only		Ndc 0078-0385-66 (Myfortic 02)
Myfortic 180 mg delayed-release tablets label by Novartis Pharmaceuticals Corporation. The label shows the product name, active ingredient mycophenolic acid, strength of 180 mg, oral dosage form, and package size of 120 tablets. It includes instructions to dispense the accompanying Medication Guide and indicates Rx only.*
FDA Label Image

Principal Display Panelpackage Label – 360 mgrx Only Ndc 0078-0386-66 (Myfortic 03)

Principal Display Panelpackage Label – 360 mgrx Only		Ndc 0078-0386-66 (Myfortic 03)
Myfortic 360 mg delayed-release tablets label by Novartis Pharmaceuticals Corporation. This oral prescription drug contains mycophenolic acid as mycophenolate sodium. The label indicates a bottle of 120 tablets with dosing information and medication guide instructions included.*

* 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.