Mitomycin Injection, Powder, Lyophilized, For Solution
Product Images NDC 25021-251

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mitomycin (NDC 25021-251). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

Figure (Mit0a 0000 01)

Figure (Mit0a 0000 01)
Chemical structure diagram of Mitomycin, illustrating its detailed molecular framework with labeled chemical groups visible in the image.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Mit0a 0000 02)

Package Label – Principal Display Panel – Vial Label (Mit0a 0000 02)
Mitomycin for Injection, USP 5 mg per vial label shows it as a single-dose vial of lyophilized powder for injection. The label highlights it is for intravenous use and must be administered intravenously to avoid tissue damage. It bears warnings about cytotoxicity and storage instructions, and the labeler is Sagent Pharmaceuticals.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Mit0a 0000 03)

Package Label – Principal Display Panel – Vial Label (Mit0a 0000 03)
Mitomycin for Injection, USP 20 mg per vial, single-dose vial. The label indicates it is a sterile, preservative-free lyophilized powder for intravenous administration. It contains mitomycin dissolved by adding sterile water. The labeler is Sagent Pharmaceuticals. Storage and handling instructions are provided with caution that it is a cytotoxic agent.*

* 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.