Daptomycin Injection, Powder, Lyophilized, For Solution
Product Images NDC 71839-108

4 FDA label images from Be Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Daptomycin (NDC 71839-108). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Be Pharmaceuticals 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
FDA Label Image

Daptocartonlabel1vial (Daptocartonlabel1vial)

Daptocartonlabel1vial (Daptocartonlabel1vial)
Packaging label for Daptomycin for Injection 350 mg per vial, lyophilized powder for solution. The label states the product must be refrigerated and reconstituted with 7 mL of 0.9% sodium chloride injection to obtain a concentration of 50 mg/mL. It is for intravenous use only and distributed by BE Pharmaceuticals Inc. The label includes barcode, storage instructions, and dosage preparation information.*
FDA Label Image

Daptostr (Daptostr)

Daptostr (Daptostr)
Chemical structure of daptomycin, a cyclic lipopeptide antibiotic composed of multiple amino acid residues and a lipophilic tail. The diagram shows the molecular arrangement relevant to its antibiotic activity.*
FDA Label Image

Daptoviallabel (Daptoviallabel)

Daptoviallabel (Daptoviallabel)
Label for daptomycin for Injection 350 mg per vial, a lyophilized powder for intravenous use. The label specifies it must be refrigerated, reconstituted with 7 mL of 0.9% sodium chloride, and is single-dose. Distributed by BE Pharmaceuticals Inc., made in India, with storage instructions and a barcode 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.