Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 70594-123

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 Vancomycin Hydrochloride (NDC 70594-123). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xellia Pharmaceuticals Usa 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 (Vancomycin 01)

Chemical Structure (Vancomycin 01)
Chemical structure of vancomycin hydrochloride, showing its complex molecular arrangement with multiple rings, hydroxyl, amino, and chlorine functional groups.*
FDA Label Image

Principal Display Panel (1 gram Vial Carton)

Principal Display Panel (1 gram Vial Carton)
Packaging label for Vancomycin Hydrochloride for Injection, USP 1 gram per vial, powder, lyophilized, for intravenous use. The label shows the product is preservative-free and sterile, with a package size of 10 x 1 g vials. Manufactured for Xellia Pharmaceuticals USA LLC. The label includes preparation instructions stating the drug must be further diluted before use and storage guidelines after reconstitution.*
FDA Label Image

Principal Display Panel (500 mg Vial Carton)

Principal Display Panel (500 mg Vial Carton)
Packaging label for Vancomycin Hydrochloride for Injection, USP, 500 mg per vial. The product is a preservative-free, sterile, lyophilized powder for intravenous use, supplied as 10 vials of 500 mg each. Labeler is Xellia Pharmaceuticals USA LLC. The label includes usage instructions and storage information.*

* 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.