Gleolan Powder, For Solution
Product Images NDC 59137-231

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Gleolan (NDC 59137-231). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medexus Pharma, 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

Chemical Structure (Gleolan 01)

FDA Label Image

Principal Display Panel (1,500 mg Vial Carton)

Principal Display Panel (1,500 mg Vial Carton)
This is a description of a medication named Gleolan. It is a single-dose vial oral solution containing 1,500mg of aminolevulinic acid hydrochloride. The solution needs to be reconstituted before use and any unused portion should be discarded. Each mL of reconstituted solution contains 30mg of aminolevulinic acid hydrochloride. The minimum and maximum storage temperature for the medication are 5 °C and 30 °C, respectively. The medication needs to be used within 24 hours of reconstitution. Dosage and Administration information are available but not provided in this text.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.