Droperidol Injection, Solution
Product Images NDC 0517-9702
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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.
Container (Droperidol Injection Usp 2)
This is a medication called "NIECTON". It comes in a single dose vial of 2 mL and has a concentration of 5 mg/2 mL (2.5 mg/mL). It is meant for intravenous use only and is an allergy medication. The vial should be protected from light and there are no preservatives. Directions for use can be found in the package insert, and any unused portion should be discarded. Information on the lot and expiration date is not available.*
Carton (Droperidol Injection Usp 3)
Droperidol is an injectable solution for intravenous or intramuscular use that comes in a 25 x 2 mL pack, with each vial containing 5 mg/2 mL of the solution. The solution contains Droperidol, Water for Injection q.s. pH adjusted with Lactic Acid and, if necessary, with Sodium Hydroxide. It does not contain any preservatives, and the unused portion should be discarded. It must be protected from light and stored in the carton until used, within the temperature range of 20°-25°C (68°-77°F), with excursions permitted to 15%-30°C (59°-86°F). Directions for use can be found in the package insert. This was manufactured by American Regent, Inc. in Shirley, NY, and the lot/exp numbers are not available.*
Droperidol Injection Usp 4
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.