Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride Injection
Product Images NDC 0781-3493

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride (NDC 0781-3493). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz Inc., 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

Structure (Dex Rtu 01)

Chemical structure of dexmedetomidine hydrochloride, showing the molecular arrangement including an imidazole ring, aromatic ring with methyl groups, and hydrochloride salt component.*

FDA Label Image

80mcg (Dex Rtu 02)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 4 mcg/mL (80 mcg per 20 mL) single-dose vial for intravenous infusion. The label states the vial size is 20 mL and instructs to discard unused portion. Manufactured by Sandoz Inc. and Jiangsu Hengrui Pharmaceuticals, the label includes storage and handling instructions and a barcode.*

FDA Label Image

200mcg (Dex Rtu 03)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 4 mcg/mL strength, provided in a 50 mL single-dose intravenous infusion bottle. The label indicates it is for intravenous use only, sterile, nonpyrogenic, preservative-free, and includes storage instructions. Manufactured by Sandoz Inc.*

FDA Label Image

400mcg (Dex Rtu 04)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg (base) per 100 mL (4 mcg per mL), intravenous injection in a 100 mL single-dose bottle. Produced by Sandoz Inc., the label includes storage instructions, dosage form, bar code, and manufacturing details from Jiangsu Hengrui Pharmaceuticals.*

* 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.