Dexmedetomidine Hydrochloride Injection
Product Images NDC 68083-239

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride (NDC 68083-239). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

Dexmedetomidine-hcl-chemical-structure (Dexmedetomidine HCl Chemical Structure)

Chemical structure of Dexmedetomidine Hydrochloride showing its molecular framework including an imidazole ring and a chlorinated aromatic ring.*

FDA Label Image

Dexmedetomidine-hcl-50-ml-label (Dexmedetomidine HCl 50 mL Label)

Label for Dexmedetomidine Hydrochloride Injection 4 mcg/mL (200 mcg/50 mL) single-dose vial for intravenous infusion. Contains 50 mL vial. Includes active ingredient concentration, NDC 68083-238-01, storage instructions at 20 to 25°C, preservative-free statement, and manufacturer information from Gland Pharma Limited, Hyderabad, India.*

FDA Label Image

Dexmedetomidine-hcl-50-ml-carton (Dexmedetomidine HCl 50 mL Carton)

This is a carton label for Dexmedetomidine Hydrochloride Injection 200 mcg/50 mL (4 mcg/mL) in 0.9% Sodium Chloride for intravenous infusion. The label states it is a single-dose vial and preservative-free, manufactured by Gland Pharma Limited. The package contains 20 units of 50 mL each, with the NDC 68083-238-20.*

FDA Label Image

Dexmedetomidine-hcl-100-ml-label (Dexmedetomidine HCl 100 mL Label)

Label for Dexmedetomidine Hydrochloride Injection 400 mcg/100 mL (4 mcg/mL) single-dose vial for intravenous infusion. The vial contains 100 mL and is labeled for Rx use only. Manufactured by Gland Pharma Limited, with storage instructions and barcode shown.*

FDA Label Image

Dexmedetomidine-hcl-100-ml-carton (Dexmedetomidine HCl 100 mL Carton)

Packaging label for Dexmedetomidine Hydrochloride 4 mcg/mL injection in 100 mL single-dose vials, containing 400 mcg per vial. The label states it is for intravenous infusion, preservative-free, and includes storage instructions at 20°C to 25°C. The label is from Gland Pharma Limited and includes an NDC of 68083-239-10 with a barcode and manufacturer details.*

FDA Label Image

Dexmedetomidine-spl-pouch-label-400mcg (Dexmedetomidine Spl Pouch Label 400mcg)

Label for Dexmedetomidine Hydrochloride Injection 4 mcg/mL in 0.9% Sodium Chloride, 100 mL single-dose flexible container for intravenous infusion. Manufactured by Gland Pharma Limited, Hyderabad, India. Label includes dosage concentration, storage instructions, and warnings about use and packaging integrity, with a barcode and manufacturer details.*

FDA Label Image

Dexmedetomidine-spl-infusion-bag-label-400mcg (Dexmedetomidine Spl Infusion Bag Label 400mcg)

Label for Dexmedetomidine Hydrochloride Injection 4 mcg/mL (400 mcg per 100 mL) in 0.9% Sodium Chloride, presented in a 100 mL single-dose flexible container. For intravenous infusion, ready-to-use, sterile, and nonpyrogenic. Manufactured by Gland Pharma Limited, Hyderabad, India. The label includes dosage instructions, storage conditions, and a barcode.*

FDA Label Image

Dexmedetomidine-spl-carton-label-400mcg (Dexmedetomidine Spl Carton Label 400mcg)

Packaging label for Dexmedetomidine Hydrochloride 4 mcg/mL injection in 0.9% Sodium Chloride, produced by Gland Pharma Limited. The label shows it is for intravenous infusion, sterile, nonpyrogenic, supplied in 10 single-dose 100 mL flexible containers. The label warns not to dilute and not to remove the unit from the overwrap until ready to use.*

* 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.