Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9356

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 0143-9356). 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 500 mg And 1)

Chemical structure of Vancomycin Hydrochloride, illustrating the distinct molecular arrangement of atoms and functional groups in this antibiotic compound.*

FDA Label Image

500 mg Container Plb257 (Vancomycin Hydrochloride For Injection 500 mg And 2)

Vancomycin Hydrochloride for Injection, USP 500 mg per vial label for intravenous use. The label shows it is preservative free and includes a warning that after reconstitution the solution must be further diluted before use. It is labeled Rx only and manufactured by Hikma Pharmaceuticals USA Inc. The vial contains lyophilized powder for solution.*

FDA Label Image

500 mg Shelfpack Plb260 (Vancomycin Hydrochloride For Injection 500 mg And 3)

Label for Vancomycin Hydrochloride for Injection, USP, 500 mg per vial, a lyophilized powder for intravenous use. The package contains 25 vials of 500 mg each. The label notes the product is preservative free and requires further dilution after reconstitution. It includes storage instructions and manufacturer information, Hikma Pharmaceuticals USA Inc.*

FDA Label Image

1 Gram Container Plb258 (Vancomycin Hydrochloride For Injection 500 mg And 4)

Label for Vancomycin Hydrochloride for Injection, USP, 1 g per vial, preservative free, intended for intravenous use. The label advises that after reconstitution the product must be further diluted before use. It includes dilution instructions, storage conditions, labeler information (Hikma Pharmaceuticals USA Inc.), and cautionary statements. The NDC number is 0143-9357-01.*

FDA Label Image

1 Gram Shelfpack Plb261 (Vancomycin Hydrochloride For Injection 500 mg And 5)

Vancomycin Hydrochloride for Injection, USP 1 g per vial, lyophilized powder for intravenous use only. The label indicates the product is preservative free and requires further dilution after reconstitution. Packaged as 10 vials of 1 g each, distributed by Hikma Pharmaceuticals USA Inc., with storage instructions and dosage directions included.*

FDA Label Image

Serialization Image (Vancomycin Hydrochloride For Injection 500 mg And 6)

Label panel containing a QR code and text fields for GTIN, serial number (SN), expiration date (EXP), and lot number (LOT), used for product identification and tracking purposes. The fields include placeholder examples: GTIN 00301234567896, SN 1234567890123, EXP MMYYYY, and LOT ABCDE12345.*

* 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.