Mitomycin Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9279

7 FDA label images from Hikma Pharmaceuticals Usa Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Mitomycin (NDC 0143-9279). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Mitomycin Structural Formula (Mitomycin For Injection Usp 1)

Mitomycin Structural Formula (Mitomycin For Injection Usp 1)
Chemical structure of mitomycin, showing its key functional groups and ring system, depicted in a 2D molecular diagram.*
FDA Label Image

Structural Formula (Mitomycin For Injection Usp 2)

Structural Formula (Mitomycin For Injection Usp 2)
Mitomycin 40 mg/80 mL injection, powder, lyophilized, for solution, in a single-use vial. The label includes dosage strength, volume, dilution instructions, storage information, lot number, and expiration date. Manufactured by Hikma Pharmaceuticals USA Inc. The label features a blue and white color scheme with red accents and a barcode.*
FDA Label Image

Mitomycin For Injection, Usp 20 mg/vial Container Label (Mitomycin For Injection Usp 3)

Mitomycin For Injection, Usp 20 mg/vial Container Label (Mitomycin For Injection Usp 3)
Label for Mitomycin injection, USP, 20 mg/vial, lyophilized powder for intravenous solution by Hikma Pharmaceuticals USA Inc. Includes dosage strength, warnings about intravenous administration to avoid tissue damage, storage instructions, and distributor information (WEST-WARD, Eatontown, NJ). The label also shows lot and expiration details and barcode.*
FDA Label Image

Mitomycin For Injection, Usp 40 mg/vial Container Label (Mitomycin For Injection Usp 4)

Mitomycin For Injection, Usp 40 mg/vial Container Label (Mitomycin For Injection Usp 4)
Mitomycin for Injection, USP 40 mg/vial. This label is for a powder, lyophilized for solution form intended for intravenous use. The label includes warnings about administration to avoid tissue damage, dosage instructions, storage conditions, and manufacturer information. Labeler is Hikma Pharmaceuticals USA Inc., with distribution by West-Ward Pharmaceuticals.*
FDA Label Image

Mitomycin For Injection 20 mg/vial Carton Label (Mitomycin For Injection Usp 5)

Mitomycin For Injection 20 mg/vial Carton Label (Mitomycin For Injection Usp 5)
Packaging label for Mitomycin for Injection, USP, 20 mg per vial. The label includes instructions for reconstitution, storage conditions, and a warning that the drug must be administered intravenously to avoid tissue damage. Manufactured by Thymoorgan Pharmazie GmbH, distributed by West-Ward, the label highlights the lyophilized powder form and contains barcode and NDC 0143-9279-01.*
FDA Label Image

Mitomycin For Injection 40 mg/vial Carton Label (Mitomycin For Injection Usp 6)

Mitomycin For Injection 40 mg/vial Carton Label (Mitomycin For Injection Usp 6)
Packaging label for Mitomycin for Injection, USP, 40 mg per vial. The label includes storage instructions, preparation directions, and warnings to administer intravenously to avoid tissue damage. Manufactured by Thymoorgan Pharmazie GmbH and distributed by West-Ward, Eatontown, NJ. The label also states the product is Rx only.*
FDA Label Image

Representative Carton Serialization Image (Mitomycin For Injection Usp 7)

Representative Carton Serialization Image (Mitomycin For Injection Usp 7)
Label showing lot number, expiration date, a Data Matrix barcode, GTIN 00301234567896, and serial number 12345678901234 for Mitomycin injection, powder, lyophilized, for solution, manufactured by Hikma Pharmaceuticals USA Inc.*

* 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.