Dalbavancin Injection, Powder, Lyophilized, For Solution
Product Images NDC 70069-830

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dalbavancin (NDC 70069-830). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

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Image (Ed056e1e 9906 4daf 9895 A3cbcc017b09 01)
Chemical structure of Dalbavancin, a complex lipoglycopeptide antibiotic molecule. The diagram shows the molecular framework including various rings, hydroxyl groups, amide bonds, and substituents represented by R1 and R2, as well as the 1.6 HCl designation indicating a hydrochloride salt form.*
FDA Label Image

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Label for Dalbavancin 500 mg per vial injection powder, lyophilized for solution, intended for intravenous infusion only. The label indicates sterile single-dose vial packaging and provides reconstitution and dilution instructions, storage conditions, and manufacturing details by Somerset Therapeutics, LLC. The product NDC is 70069-830.*
FDA Label Image

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Image (Ed056e1e 9906 4daf 9895 A3cbcc017b09 03)
Carton label for Dalbavancin injection powder, lyophilized, for solution, 500 mg per vial, for intravenous use only. The label indicates a sterile single-dose vial and includes storage conditions, reconstitution instructions, and handling precautions. The labeler is Somerset Therapeutics LLC, with NDC 70069-830. The label displays barcodes, regulatory text including Rx only, and manufacturing information stating the product is made in India.*

* 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.