Mycophenolate Mofetil Tablet, Film Coated
Product Images NDC 70518-4377

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mycophenolate Mofetil (NDC 70518-4377). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Structural Formula (2dab9b9d D85e 46f3 9518 C9f6e4fbf70e 01)

Structural Formula (2dab9b9d D85e 46f3 9518 C9f6e4fbf70e 01)
Chemical structure of mycophenolate mofetil, depicting its molecular arrangement with specific functional groups including a substituted aromatic ring, ester linkages, and a morpholine ring.*
FDA Label Image

Mm2 (Mycophenolate Mofetil 500mg 70518 4377 01)

Mm2 (Mycophenolate Mofetil 500mg 70518 4377 01)
Mycophenolate mofetil 500 mg tablet label showing a single film-coated tablet dosage form. The label includes NDC 70518-4377-01 and is repackaged by RemedyRepack Inc., Indiana, PA. It features storage instructions, manufacturer information (Avet Pharma, East Brunswick, NJ), and dosage guidance to see the insert. The label highlights that the product is prescription only (RX ONLY).*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Mycophenolate mofetil 500 mg tablet label displaying quantity of 100 per box. The label shows that the product is repackaged by RemedyRepack Inc., Indiana, PA. It includes storage instructions, manufacturer information (Avet Pharma, East Brunswick, NJ), and cautions to keep the medication out of reach of children. The tablet is identified as a brown capsule on the label.*

* 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.