Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride Injection, Solution
Product Images NDC 25021-615

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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 25021-615). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

Figure (Dex1t 0001 01)

Figure (Dex1t 0001 01)
Chemical structure of dexmedetomidine hydrochloride, showing a bicyclic imidazole and aromatic ring with methyl groups and a hydrochloride salt component.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Dex1t 0001 02)

Package Label – Principal Display Panel – Vial Label (Dex1t 0001 02)
Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg per mL), in a 50 mL single-dose bottle for intravenous use. The label includes storage instructions, manufacturer Sagent Pharmaceuticals, and a barcode.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Dex1t 0001 03)

Package Label – Principal Display Panel – Vial Label (Dex1t 0001 03)
Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg per mL) solution. The label indicates a 100 mL single-dose bottle for intravenous use, manufactured by Sagent Pharmaceuticals. It states the product is sterile, nonpyrogenic, preservative-free, and contains 4 mcg/mL of dexmedetomidine hydrochloride in 0.9% sodium chloride solution.*

* 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.