Dexmedetomidine Hydrochloride Injection, Solution
Product Images NDC 42023-187

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride (NDC 42023-187). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Par Health Usa, 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

Chemical Structure (Image 1)

FDA Label Image

Principal Display Panel (25 Vial Carton)

Principal Display Panel (25 Vial Carton)
This is a product label for Dexmedetomidine, an injection solution for intravenous use. The solution contains 200 micrograms of the drug per 2 milliliters of the solution. The label emphasizes that the solution should be diluted before use and provides instructions for use.*
FDA Label Image

20 X 50 mL Carton (Image 3)

20 X 50 mL Carton (Image 3)
This is a product description of a medication called Dexmedetomidine Hcl with a recommended dosage indicated in the full prescribing information. It is provided in a 50 mL single-dose vial with 4 mg of dexmedetomidine per mL mixed with 9 mg of sodium chloride in water for injection. Users should not freeze it but instead store it at room temperature between 20°C to 25°C (68°F to 77°F). The medication is meant for intravenous infusion and should be discarded if any portion is unused.*
FDA Label Image

10 X 100 mL Carton (Image 4)

10 X 100 mL Carton (Image 4)
This is a product description for Dexmedetomidine HCI in 0.9% Sodium Chloride Injection, a solution for intravenous infusion packaged in 10 x 100 mL single-dose vials. Each mL contains 4 mcg of dexmedetomidine, which is intended for sedating patients before and during surgical and other procedures. It is distributed by Par Pharmaceutical and should be stored at controlled room temperature. The vial stopper does not contain natural rubber latex. The text also includes a National Drug Code (NDC) identifier.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.