Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 0404-9965

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 0404-9965). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

Formula1.jpg (Formula1)

Chemical structure diagram of Vancomycin Hydrochloride, showing the arrangement of molecular components including rings, hydroxyl groups, amine groups, and chlorine atoms with an associated HCl component.*

FDA Label Image

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A dosage table showing vancomycin dosing in mg/24 h according to creatinine clearance rates in mL/min for patients with impaired renal function. The table lists decreasing creatinine clearance from 100 to 10 mL/min with corresponding vancomycin doses ranging from 1,545 mg to 155 mg.*

FDA Label Image

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A data table illustrating formulas for calculating a value based on weight, age, and serum creatinine concentration. It shows separate calculations for men and women, with women's values adjusted by multiplying men's result by 0.85. The units for serum creatinine concentration are mg/dL.*

FDA Label Image

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A table presenting Vancomycin Hydrochloride injection concentrations per vial alongside the corresponding volumes of diluent for reconstitution. It lists 500 mg with 10 mL, 750 mg with 15 mL, and 1 g with 20 mL of diluent volume.*

FDA Label Image

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Label for Vancomycin Hydrochloride Injection USP sterile powder, 500 mg strength. The label indicates it is a lyophilized powder for intravenous use, requiring dilution before use. Manufacturer is Henry Schein, Inc., located in Bastian, VA. The label includes storage instructions, warnings, lot, expiration placeholders, and an NDC barcode 0404-9965-99.*

* 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.