Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 72572-029

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 72572-029). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Chemical Structure (Vancomycin 01)

Chemical structure of vancomycin hydrochloride, showing its detailed molecular arrangement including various ring structures, hydroxyl groups, amino groups, and chlorine atoms.*

FDA Label Image

Civica Logo (Vancomycin 02)

FDA Label Image

Principal Display Panel (1 g Vial Label)

Vancomycin Hydrochloride for Injection, USP 1 g vial lyophilized powder for intravenous use by Civica, Inc. The label indicates it is a single-dose fliptop vial requiring further dilution before use. Instructions highlight dilution with 20 mL sterile water and refrigeration after dilution. Manufactured by Hospira, Inc.*

FDA Label Image

Principal Display Panel (1 g Vial Carton)

Packaging label for Vancomycin Hydrochloride for Injection, USP sterile powder, equivalent to 1 g/vial Vancomycin. The label specifies it is for intravenous use and comes in single-dose fliptop vials, with 10 units per package. Distributed by Civica, Inc., manufactured by Hospira, Inc., and made in Italy. The label emphasizes the need for further dilution before use and includes the product NDC 72572-029-10.*

* 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.