Micafungin Injection, Powder, Lyophilized, For Solution
Product Images NDC 63323-729

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Micafungin (NDC 63323-729). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, 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

Micaf-struc-01.jpg (Micaf Struc 01)

Chemical structure of micafungin sodium, depicted as a complex molecular diagram illustrating its chemical bonds and atom arrangement.*

FDA Label Image

Micaf-img-01.jpg (Micaf Img 01)

FDA Label Image

Micaf-label-01.jpg (Micaf Label 01)

Micafungin for Injection label displaying a 50 mg per vial strength of lyophilized powder for intravenous use. The label includes dosage information, storage instructions, and a barcode. The product is manufactured by Fresenius Kabi USA, LLC and specifies single dose vial use with a caution to discard unused portion.*

FDA Label Image

Micaf-label-02.jpg (Micaf Label 02)

Packaging label for Micafungin for Injection, 50 mg per vial, a lyophilized powder for intravenous injection. Manufactured for Fresenius Kabi USA, LLC. The label includes dosage strength, storage instructions, sterile powder details, and usage precautions. The package size is noted as a single dose vial, with barcodes and website information for Fresenius Kabi.*

FDA Label Image

Micaf-label-03.jpg (Micaf Label 03)

Micafungin for Injection 50 mg per vial lyophilized powder for solution, shown on a carton label with the indication for intravenous infusion only. The packaging indicates single dose vials, 10 vials per carton, labeled by Fresenius Kabi USA, LLC. The label includes storage instructions, preservative status, and a website link for more information.*

FDA Label Image

Micaf-label-04.jpg (Micaf Label 04)

Micafungin 100 mg per vial injection label for intravenous use. The label identifies the product as Micafungin for Injection, 100 mg per vial, a lyophilized powder for solution. It includes usage instructions to discard unused portions and storage conditions to store at 25°C with specified excursions. The label is from Fresenius Kabi USA, LLC and features a barcode, lot, and expiration date fields, with a pull tab indicated for opening.*

FDA Label Image

Micaf-label-05.jpg (Micaf Label 05)

Packaging label for Micafungin for Injection 100 mg per vial, a lyophilized powder for intravenous use. The label includes the NDC number 63323-729-01 and states the product is sterile, preservative-free, and intended for single-dose use. It is manufactured for Fresenius Kabi USA, LLC with storage instructions and a printed lot number and expiration date area.*

FDA Label Image

Micaf-label-06.jpg (Micaf Label 06)

Micafungin 100 mg per vial injection powder, lyophilized for intravenous infusion. The label specifies it is for injection only with discard unused portion instructions. Contents include 10 single-dose vials of 100 mg each. The labeler is Fresenius Kabi USA, LLC, including storage instructions and contact information. Barcode and NDC 63323-729-10 are visible.*

* 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.