Daptomycin Injection, Powder, Lyophilized, For Solution
Product Images NDC 55150-344

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Daptomycin (NDC 55150-344). 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.

FDA Label Image

Chemical Structure (Daptomycin Str)

Chemical structure diagram of Daptomycin, illustrating the molecular arrangement of atoms and bonds within the active ingredient. The structure highlights various functional groups and the cyclic peptide framework characteristic of daptomycin.*

FDA Label Image

Package Label-principal Display Panel-500 mg Per Vial (Container Label)

Label for Daptomycin for Injection, 500 mg per vial, lyophilized powder for solution, intended for intravenous infusion. The label emphasizes storage requirements, stating the product must be refrigerated at 2°C to 8°C (36°F to 46°F). It also instructs to use 10 mL of 0.9% Sodium Chloride Injection for reconstitution and to discard unused portions. The labeler is AuroMedics Pharma LLC, with manufacturing in India.*

FDA Label Image

Package Label-principal Display Panel-500 mg Per Vial – Container-carton Label (Daptomycin Fig2)

Packaging label for Daptomycin injection, 500 mg per vial, lyophilized powder for reconstitution. The product is for intravenous infusion and requires reconstitution with 10 mL 0.9% Sodium Chloride Injection. The label instructs that the vial must be refrigerated at 2°C to 8°C (36°F to 46°F). It is a single-dose vial distributed by Auromedics Pharma LLC and made in India. The label includes NDC 55150-344-01 and barcode, with directions to discard unused portions.*

* 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.