Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride Injection
Product Images NDC 84549-493

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride (NDC 84549-493). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Propharma Distribution, 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

Label (84549 493 95)

Label (84549 493 95)
Label for Precedex Dexmedetomidine Injection USP, 80 mcg in a 20 mL single-dose vial for intravenous infusion. The label states it is sterile, nonpyrogenic, preservative-free, and includes storage instructions at 25°C with permitted excursions. It lists packaging by ProPharma Distribution LLC in Westminster, CO. The label includes an NDC barcode and space for lot and expiration dates.*
FDA Label Image

Structure (Dex Rtu 01)

Structure (Dex Rtu 01)
Chemical structure diagram of dexmedetomidine hydrochloride, showing the molecular arrangement including methyl groups and an imidazole ring.*
FDA Label Image

Table3 (Table3)

Table3 (Table3)
A data table listing adverse reactions with an incidence greater than 2% in adult intensive care unit sedation populations treated for less than 24 hours. It compares incidence percentages for Dexmedetomidine (all and randomized groups), Placebo, and Propofol across various adverse events such as hypotension, hypertension, nausea, bradycardia, atrial fibrillation, and others.*

* 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.