Mycophenolate Mofetil Injection, Powder, Lyophilized, For Solution
Product Images NDC 83270-000

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mycophenolate Mofetil (NDC 83270-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Onesource Specialty Pharma Limited, 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 lyophilized powder for intravenous infusion. The label indicates 4 single-dose vials per package, with instructions to dispense the accompanying medication guide. Labeler information includes Steriscience Pte. Ltd and distribution by Armas Pharmaceuticals, Inc. Dimensions specified as 74 x 74 x 80 mm.*

FDA Label Image

Structure (Mycophenolate Mofetil For Injection Usp 1)

Chemical structure diagram of mycophenolate mofetil, a pharmaceutical active ingredient.*

FDA Label Image

Vial-label-image (Vial Label Image)

The label is for Mycophenolate Mofetil for Injection, USP, 500 mg per vial, intended for intravenous infusion. It specifies a single-dose vial containing 500 mg of mycophenolate mofetil, with stability and storage instructions provided. The label also includes the NDC 72485-415-01, manufacturer Stelis Biopharma Limited in India, and distributor Armas Pharmaceuticals, Inc. in the USA. Additional directions for pharmacists about dispensing the medication guide are present.*

* 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.