Micafungin Injection, Powder, Lyophilized, For Solution
Product Images NDC 25021-191

3 FDA label images from Sagent Pharmaceuticals · 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 Micafungin (NDC 25021-191). 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

Chemical Structure Of Micafungin Sodium (Mic19 0000 01)

Chemical Structure Of Micafungin Sodium (Mic19 0000 01)
Chemical structure diagram of Micafungin Sodium, showing its molecular bonds and atomic arrangement typical of a complex antifungal agent.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Mic19 0000 02)

Package Label – Principal Display Panel – Vial Label (Mic19 0000 02)
Micafungin for Injection 50 mg per vial lyophilized powder for solution. Label states each mL contains 10 mg micafungin after reconstitution. It is for intravenous infusion only, single-dose vial, and instructs to discard unused portion. Manufactured by Sagent Pharmaceuticals with storage and dosage instructions included on the label.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Mic19 0000 03)

Package Label – Principal Display Panel – Vial Label (Mic19 0000 03)
Micafungin 100 mg per vial injection powder label for intravenous use by Sagent Pharmaceuticals. The single-dose vial contains lyophilized powder for reconstitution, with each mL of solution providing 20 mg micafungin. The label indicates it is sterile, preservative-free, and specifies storage conditions and dosing instructions.*

* 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.