Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 43538-805

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 43538-805). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eurofarma, 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 (Vancomicina 01)

Chemical Structure (Vancomicina 01)
Chemical structure diagram of Vancomycin hydrochloride showing its molecular arrangement with atoms and bonds, including hydroxyl, amino, chlorine groups, and associated hydrochloride (HCl) component.*
FDA Label Image

Principal Display Panel (1 g Vial Carton)

Principal Display Panel (1 g Vial Carton)
Packaging label for Vancomycin Hydrochloride 1 gram per vial injection, USP, from Medimetriks Pharmaceuticals, Inc. The label indicates the product is for intravenous use, preservative-free, and must be further diluted before use. The package contains 10 vials of 1 gram each. Manufactured by Eurofarma Laboratories S.A. in Brazil and distributed by Medimetriks Pharmaceuticals, Inc. in New Jersey, USA.*
FDA Label Image

Principal Display Panel (500 mg Vial Carton)

Principal Display Panel (500 mg Vial Carton)
Vancomycin Hydrochloride 500 mg injection powder vial label for intravenous use. The label indicates the product is preservative free and must be further diluted before use. It includes 10 vials per package, each vial containing 500 mg equivalent of Vancomycin. Manufactured by Eurofarma Laboratories S.A., Brazil, and distributed by Medimetriks Pharmaceuticals, 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.