Gentamicin Sulfate Injection, Solution
Product Images NDC 0404-9865

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Gentamicin Sulfate (NDC 0404-9865). 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 of Gentamicin Sulfate showing its molecular arrangement and functional groups, including variations in the R group for different components (C1, C2, C1A) as labeled alongside the main molecular structure.*

FDA Label Image

Image1.jpg (Image1)

A dosage schedule guide table for Gentamicin Sulfate Injection, Solution 40 mg/mL for adults with normal renal function. It details dosing at eight-hour intervals based on patient's weight in kilograms and pounds, showing usual doses for serious infections and higher doses for life-threatening infections in mg per dose and mL per dose, along with footnotes about dose considerations for obese patients and recalculation for q8h schedules.*

FDA Label Image

Image2.jpg (Image2)

A dosage adjustment guide table for Gentamicin Sulfate Injection, Solution, indicating recommended dose percentages at eight-hour intervals based on patients' serum creatinine levels (mg %) and approximate creatinine clearance rates (mL/min/1.73m²) to facilitate dosing for renal impairment.*

FDA Label Image

Image3.jpg (Image3)

A data table listing unit of sale and concentration for Gentamicin Sulfate injection. The unit of sale is 25 vials in a tray with NDC 0409-1207-03. The concentration is 80 mg per 2 mL, equivalent to 40 mg/mL.*

FDA Label Image

Label1.jpg (Label1)

Label of Gentamicin Sulfate injection, 80 mg/2 mL (40 mg/mL) single dose vial for intramuscular and intravenous use. The label includes storage instructions (65°F to 77°F), manufacturer information (packaged by Henry Schein, Inc., Bastian, VA), and a barcode with NDC 0404-9865-02. It states the product must be diluted for intravenous use and is restricted to prescription only (Rx only).*

* 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.