Mycophenolate Mofetil
Product Images NDC 60687-494

4 FDA label images from American Health Packaging · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mycophenolate Mofetil (NDC 60687-494). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Ahp49401

Ahp49401
Mycophenolate Mofetil capsules by American Health Packaging feature a two-tone design with one half blue and the other half orange. The capsules are imprinted with the code '54 848' on the blue and orange halves, shown from two angles on a measurement grid background.*
FDA Label Image

Blister

Blister
Sheet of labels for Mycophenolate Mofetil Capsule USP 250 mg from American Health Packaging. Each label includes the product name, strength, a barcode, and placeholder text for expiration date and lot number, with the company's location in Columbus, Ohio.*
FDA Label Image

Carton

Carton
Mycophenolate Mofetil Capsules USP, 250 mg, packaged in a 100-count (10 x 10) bottle. The label includes the NDC 60687-494-01, pharmacist instructions to dispense with the Medication Guide, storage and handling information, a caution about protective measures, and the packaging and distribution by American Health Packaging, Columbus, Ohio.*
FDA Label Image

Structure

Structure
Chemical structure diagram of the active ingredient Mycophenolate Mofetil, showing its molecular framework with annotated functional groups and bonds.*

* 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.