Dexmedetomidine Injection, Solution
Product Images NDC 55150-209

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine (NDC 55150-209). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us Llc, 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

Package Label-principal Display Panel (200 mcg per 2 mL (100 mcg/mL))

Label for Dexmedetomidine Injection, USP 200 mcg per 2 mL (100 mcg/mL) intravenous solution. The product is a 2 mL single-dose vial concentrated and must be diluted prior to use. It is distributed by AuroMedics Pharma LLC, made in India, and marked for prescription use only.*

FDA Label Image

Package Label-principal Display Panel (200 mcg per 2 mL (100 mcg/mL))

Packaging label for Dexmedetomidine Injection, USP 200 mcg per 2 mL (100 mcg/mL) by Auromedics. The sterile, nonpyrogenic intravenous injection is preservative-free and supplied in 25 single-dose vials of 2 mL each. The label notes it is a concentrate that must be diluted, with storage instructions and distributor information for AuroMedics Pharma LLC, made in India.*

FDA Label Image

Dexmedetomidine-figure3 (Dexmedetomidine Fig3)

Label for Dexmedetomidine HCl injection solution in 0.9% Sodium Chloride, 200 mcg per 50 mL (4 mcg/mL) for intravenous infusion. The sterile product comes in a 50 mL single-dose flexible container. Manufactured in India for AuroMedics Pharma LLC, this Rx-only medication advises checking for container leaks and states it is preservative-free.*

FDA Label Image

Dexmedetomidine-figure4 (Dexmedetomidine Fig4)

Label for Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg/mL) in a single-dose 50 mL flexible container for intravenous infusion. The label includes usage instructions, cautions, storage conditions, and distributor information indicating AuroMedics Pharma LLC with the product made in India.*

FDA Label Image

Dexmedetomidine-figure5 (Dexmedetomidine Fig5)

Label for Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg/mL) solution for intravenous infusion. The label notes the product is ready to use and should not be diluted. Packaging includes detailed usage caution, storage instructions, and distributor information, listing AuroMedics Pharma LLC. Barcode and recycling symbol are visible on the label.*

FDA Label Image

Dexmedetomidine-figure6 (Dexmedetomidine Fig6)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, solution for intravenous infusion, with a concentration of 400 mcg per 100 mL (4 mcg/mL). The label indicates a 100 mL single-dose flexible container, sterile, preservative-free, and contains usage and storage instructions. Manufactured for AuroMedics Pharma LLC, E. Windsor, NJ.*

FDA Label Image

Dexmedetomidine-figure7 (Dexmedetomidine Fig7)

Label for Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in a 100 mL single dose flexible container. Intended for intravenous infusion, sterile and preservative-free. Distributed by AuroMedics Pharma LLC, made in India. Includes usage and storage instructions, barcode, and handling cautions.*

FDA Label Image

Dexmedetomidine-figure8 (Dexmedetomidine Fig8)

Label for Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) for intravenous infusion. The product is presented in 10 x 100 mL single dose flexible containers and distributed by AuroMedics Pharma LLC, made in India. The label includes usage instructions, warnings, storage conditions, and recycling symbols.*

FDA Label Image

Dexmedetomidine Hydrochloride Chemical Stucture (Dexmedetomidine Str)

Chemical structure of Dexmedetomidine Hydrochloride, showing the molecular arrangement including aromatic rings and relevant functional groups as part of the hydrochloride salt form.*

* 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.