Dexmedetomidine Hydrochloride
Product Images NDC 63323-671

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride (NDC 63323-671). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi 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

Dex0z 0002 01

Chemical structure diagram of dexmedetomidine hydrochloride showing its molecular arrangement with labeled chemical groups, including methyl, imidazole, and benzene rings.*

FDA Label Image

Dex0z 0002 02

FDA Label Image

Dex0z 0002 03

Label for Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, showing a strength of 80 mcg per 20 mL (4 mcg per mL). The product is a 20 mL single-dose vial intended for intravenous infusion, preservative-free. The label includes the National Drug Code 63323-671-02 and is from Fresenius Kabi USA, LLC, Lake Zurich, IL. Storage instructions and ingredient details are also visible.*

FDA Label Image

Dex0z 0002 04

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection by Fresenius Kabi USA, LLC. The product is an 80 mcg per 20 mL (4 mcg per mL) intravenous infusion solution, preservative free, supplied in single dose vials of 20 mL each, with a package size of 10 vials. The label includes storage instructions and ingredient details.*

FDA Label Image

Dex0z 0002 05

Label for Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg per mL), from Fresenius Kabi USA, LLC. The 50 mL single-dose bottle is preservative free and intended for intravenous infusion. The label includes storage instructions, dosage notice, and manufacturing details.*

FDA Label Image

Dex0z 0002 06

Dexmedetomidine Hydrochloride Injection in 0.9% Sodium Chloride, 200 mcg per 50 mL (4 mcg per mL) single dose bottles. The label shows the product is preservative-free, for intravenous infusion, manufactured by Fresenius Kabi USA, LLC. Storage instructions and formulation details are included, along with the NDC 63323-671-50.*

FDA Label Image

Dex0z 0002 07

Label for Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg per mL), single dose bottle. The label displays formulation details, use for intravenous infusion, preservative-free statement, storage instructions, and company information for Fresenius Kabi USA, LLC. Includes barcode and lot/expiration space.*

FDA Label Image

Dex0z 0002 08

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection by Fresenius Kabi USA, LLC. The product strength is 400 mcg per 100 mL (4 mcg per mL). Packaging indicates 10 single dose bottles, each 100 mL. The label notes intravenous infusion use, preservative-free formulation, and storage instructions at 20 to 25°C. Barcodes and NDC 63323-671-00 are visible.*

* 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.