Dexmedetomidine Hydrochloride Injection, Solution
Product Images NDC 70069-759

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride (NDC 70069-759). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

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Chemical structure diagram of Dexmedetomidine Hydrochloride showing its molecular configuration with labeled carbon and nitrogen atoms and a hydrochloride (HCl) group.*

FDA Label Image

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Label for Dexmedetomidine Injection, USP 400 mcg/4 mL (100 mcg/mL) solution for intravenous use. This 4 mL multiple-dose vial is manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. The label includes product NDC, dilution instructions, and a barcode.*

FDA Label Image

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Packaging label for Dexmedetomidine Injection, USP 400 mcg/4 mL (100 mcg/mL) injection solution for intravenous use. The label indicates multiple-dose vials, 4 x 4 mL, manufactured for Somerset Therapeutics, LLC. Contains ingredients and storage instructions, with a barcode and NDC 70069-758-04.*

FDA Label Image

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Label for Dexmedetomidine Injection, USP 100 mcg/mL (1000 mcg/10 mL) intravenous solution. The label indicates a 10 mL multiple-dose vial, manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. It includes instructions that the solution must be diluted before use. The label displays NDC 70069-759-01 and a barcode.*

FDA Label Image

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Label for Dexmedetomidine Injection, USP 100 mcg/mL (1000 mcg/10 mL) intravenous solution. Pack contains 4 multiple-dose vials of 10 mL each. Manufactured for Somerset Therapeutics, LLC, with storage instructions and ingredient details including dexmedetomidine hydrochloride and preservatives. NDC 70069-759-04 is visible on the label.*

* 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.