Droperidol Injection, Solution
Product Images NDC 0517-9702

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Droperidol (NDC 0517-9702). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Regent, 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

Ad2af77a-figure-01 (Droperidol Injection Usp 1)

Chemical structure diagram of Droperidol, showing its molecular formula C22H22FN3O2 and molecular weight 379.43. The structure depicts the arrangement of atoms and bonds characteristic of the Droperidol molecule.*

FDA Label Image

Container (Droperidol Injection Usp 2)

Droperidol injection, USP 2.5 mg/mL (5 mg/2 mL) single dose vial label for intravenous or intramuscular use. The label states Rx only and is from American Regent, Inc., Shirley, NY. Instructions include protecting from light, no preservatives, and discarding unused portions. Barcode and manufacturing/revision details are present.*

FDA Label Image

Carton (Droperidol Injection Usp 3)

Droperidol injection, USP label for 5 mg/2 mL (2.5 mg/mL) solution in single dose vials. The label states it is for intravenous or intramuscular use, Rx only, with no preservatives, and includes storage instructions at controlled room temperature. Manufactured by American Regent, Inc.*

FDA Label Image

Droperidol Injection Usp 4

A product label featuring a 2D barcode and printed text with lot number, expiration date, GTIN, and serial number. The label corresponds to Droperidol injection, solution, 2.5 mg/mL by American Regent, Inc. No strength or dosage details are visible beyond the text provided.*

* 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.