Bendamustine Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 55150-392
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Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Bendamustine Hydrochloride (NDC 55150-392). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Eugia Us 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.
Product Images & Figures Index
Package Label-principal Display Panel-25 mg Per Vial (Container Label)
This is a medication with the name "Bendamustine HCI". The package contains a single dose vial with 25mg strength of Bendamustine HCI, USP and 42.5mg of Mannitol, USP. It is required to be stored at 25°C (77°F) and protected from light. The medication should be reconstituted with Sterile Water for Injection and diluted as per the instructions given in the insert. This is a cytotoxic agent and only for Intravenous Infusion. The usual dosage is to be determined by a healthcare professional.*
Package Label-principal Display Panel-25 mg Per Vial (Container-Carton (1 Vial))
This is a prescription drug called "Bendamustine Hydrochloride". It is a cytotoxic agent and should be used with caution during preparation. It is used for intravenous infusion only and requires reconstitution and dilution before use. It is available in a sterile single-dose vial containing 25 mg of Bendamustine HC1 and 42.5 mg of Mannitol. The vial stopper is not made of natural rubber latex. Recommended dosage and instructions for use are available in the insert. The drug should be stored in the original package at controlled room temperature (up to 25°C). The manufacturer is Eugia US LLC, located in New Jersey, USA.*
Package Label-principal Display Panel-100 mg Per Vial (Container Label)
This is a description of a medication called Hydrochloride for Injection, USP with 100 mg per Vial of Bendamustine HCI, USP and 170 mg Mannitol, designed as a Cytotoxic Agent for Sterile Intravenous Infusion Only. It is a Single-Dose Vial that needs reconstitution and dilution before use. Recommended Dosage can be found in the insert provided, and the medication should be Reconstituted with 20 mL of Sterile Water for Injection, USP to a concentration of 5 mg/mL. It should then be transferred immediately to either 0.9% Sodium Chloride Injection, USP or 2.5% Dextrose/0.45% Sodium Chloride Injection, USP. The medication should be stored in its original package under controlled room temperature and protected from light. Any unused portion of the medication should be discarded.*
Package Label-principal Display Panel-100 mg Per Vial (Container-Carton (1 Vial))
This is a drug information sheet for Hydrochloride for Injection, USP with NDC 55150-392-01 for intravenous infusion. It is recommended for use with caution during handling and preparation. The drug is contained within a 100mg Sterie single-dose vial and requires reconstitution with 20mL of Sterile Water for Injection, USP. The solution should be further diluted before use. This drug is a cytotoxic agent and gloves and safety glasses are recommended during handling to avoid exposure. The usual dosage should be referred to in the insert. The drug is distributed by Eugia US LLC and contains 100mg Bendamustine HCI, USP and 170mg Mannitol, USP.*
Chemical Structure (Bendamustine Str)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.