Mycophenolate Mofetil Injection, Powder, Lyophilized, For Solution
Product Images NDC 72485-415

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mycophenolate Mofetil (NDC 72485-415). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Armas Pharmaceuticals 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

Carton-label-image (Carton Label Image)

Packaging label for Mycophenolate Mofetil for Injection, USP 500 mg/vial. The product is a lyophilized powder for intravenous infusion, supplied in single-dose vials. The label includes directions for reconstitution and storage, manufacturer information listing Steriscience Pte. Ltd. and distributor Armas Pharmaceuticals, Inc. The NDC 72485-415-04 is displayed.*

FDA Label Image

Structure (Mycophenolate Mofetil For Injection Usp 1)

Chemical structure diagram of mycophenolate mofetil, showing the molecular arrangement of its atoms and bonds as related to the active pharmaceutical ingredient.*

FDA Label Image

Vial-label-image (Vial Label Image)

The label for Mycophenolate Mofetil for Injection, USP, displays 500 mg per vial in a lyophilized powder form for intravenous infusion. It includes storage instructions, dosage notes, and manufacturing details by Stelis Biopharma Limited, with distribution by Armas Pharmaceuticals, Inc. The label also highlights the Rx-only status and cautions pharmacists to dispense the accompanying medication guide.*

* 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.