Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9355

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 0143-9355). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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 Hydrochloride For Injection Usp 750 M 1)

Chemical structure of Vancomycin Hydrochloride, depicted as a complex molecular diagram with multiple rings, atoms, and bonds clearly illustrated.*

FDA Label Image

Plb207-wes.1 (Vancomycin Hydrochloride For Injection Usp 750 M 2)

Vancomycin Hydrochloride for Injection, USP 750 mg per vial powder label for intravenous use. The label states it is preservative free and must be further diluted before use. The product is distributed by Hikma Pharmaceuticals USA Inc., from Berkeley Heights, NJ, with storage instructions and dosage directions included.*

FDA Label Image

Layout 1 (Vancomycin Hydrochloride For Injection Usp 750 M 3)

Label for Vancomycin Hydrochloride for Injection, USP 750 mg per vial. It is a lyophilized powder for intravenous use that must be diluted before use. The package contains 10 vials of 750 mg each. Manufactured by Hikma Farmacêutica in Portugal and distributed by Hikma Pharmaceuticals USA Inc.*

FDA Label Image

Vancomycin Hydrochloride For Injection Usp 750 M 4

Vancomycin Hydrochloride injection powder lyophilized vial label with strength 750 mg per vial. The label shows a QR code, GTIN, serial number, expiration date, and lot number. The labeler is Hikma Pharmaceuticals USA Inc.*

* 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.