Mycophenolate Mofetil Powder, For Suspension
Product Images NDC 0527-5160

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mycophenolate Mofetil (NDC 0527-5160). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Structure (Mycophenolate Mofetil For Oral Suspension Usp 1)

Chemical structure of Mycophenolate Mofetil, showing its molecular arrangement with multiple rings, oxygen and nitrogen atoms, and functional groups as depicted in the diagram.*

FDA Label Image

Figure 1 (Mycophenolate Mofetil For Oral Suspension Usp 2)

Illustration showing components of an oral medication bottle and an oral dispenser syringe. The bottle is labeled with parts including a child-resistant bottle cap, bottle adapter, and bottle body. The oral dispenser syringe is identified with labeled parts: barrel, plunger, tip, and dosage indicators.*

FDA Label Image

Figure 2 (Mycophenolate Mofetil For Oral Suspension Usp 3)

An instructional illustration showing a person holding an oral suspension bottle inverted to pour liquid into a measuring syringe held below. The liquid is partially filled in the syringe, demonstrating proper measuring technique.*

FDA Label Image

Carton (Mycophenolate Mofetil For Oral Suspension Usp 4)

Packaging label for Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL powder for suspension, oral use. The label displays the product name and strength prominently with instructions for pharmacists on preparation. It includes storage guidelines, package contents of 175 mL, and a barcode. Distributed by Lannett Company, Inc., Philadelphia, PA.*

* 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.