Dexmedetomidine Hydrochloride Injection
Product Images NDC 70121-1712

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride (NDC 70121-1712). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

1 (Dexmedetomidine Hydrochloride In Sodium Chloride I 1)

Chemical structure of Dexmedetomidine Hydrochloride, showing a benzene ring with methyl groups and an imidazole ring, along with a hydrochloride group.*

FDA Label Image

1 (Dexmedetomidine Hydrochloride In Sodium Chloride I 2)

Label text showing manufacturing and distribution details for Dexmedetomidine Hydrochloride injection. Manufactured by Amneal Injectables Private Limited, Mehsana, India, and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ.*

FDA Label Image

1 (Dexmedetomidine Hydrochloride In Sodium Chloride I 3)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg/mL) intravenous infusion. It is a 50 mL single-dose flexible container labeled as preservative free. The product is distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ, and made in India. The label includes storage instructions, dosage form, and a barcode.*

FDA Label Image

1 (Dexmedetomidine Hydrochloride In Sodium Chloride I 4)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 4 mcg/mL (200 mcg per 50 mL), intravenous injection in a 50 mL single-dose flexible container. The label includes storage instructions, manufacturing and distribution information by Amneal Pharmaceuticals LLC and Amneal Injectables Private Limited, and notes the product is preservative-free and latex-free.*

FDA Label Image

1 (Dexmedetomidine Hydrochloride In Sodium Chloride I 5)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg/mL) intravenous injection. Packaged as 24 single-dose flexible containers of 50 mL each. Manufactured by Amneal Injectables Private Limited, India, and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. The label includes storage instructions, dosage notes, and cautions such as preservative-free and discard unused portion.*

FDA Label Image

1 (Dexmedetomidine Hydrochloride In Sodium Chloride I 6)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) intravenous infusion. The 100 mL single-dose flexible container is preservative-free and distributed by Amneal Pharmaceuticals LLC. The label includes storage instructions, manufacturing details, and a barcode.*

FDA Label Image

1 (Dexmedetomidine Hydrochloride In Sodium Chloride I 7)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 4 mcg/mL (400 mcg per 100 mL) in a 100 mL single-dose flexible container for intravenous infusion. The label indicates preservative-free formulation and manufacturing details by Amneal Injectables Private Limited, distributed by Amneal Pharmaceuticals LLC.*

FDA Label Image

1 (Dexmedetomidine Hydrochloride In Sodium Chloride I 8)

Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 4 mcg/mL (400 mcg per 100 mL) intravenous infusion. Packaged as 12 single-dose 100 mL flexible containers. Manufactured by Amneal Injectables Private Limited, India, and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. The label includes storage instructions and usage notes.*

* 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.