Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride Injection
Product Images NDC 84549-493

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This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride (NDC 84549-493). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Propharma Distribution, 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

Label (84549 493 95)

Label (84549 493 95)
This is a description of Precedex Dexmedetomidine, a prescription medication provided in an 80mcg injection USP in a 20mL single-dose vial for intravenous infusion. It is recommended to store at 25 degrees Celsius with excursions permitted between 15 to 30 degrees Celsius. The product is sterile, nonpyrogenic, and preservative-free. It should be discarded if discolored or if a precipitate is present. The manufacturer is Sandoz Inc. and it is packaged by ProPharma Distribution LLC, with prescribing information available in the manufacturer's insert.*
FDA Label Image

Structure (Dex Rtu 01)

FDA Label Image

Table3 (Table3)

Table3 (Table3)
This table provides information on adverse reactions in adult patients undergoing intensive care unit sedation for less than 24 hours. The incidence of adverse events such as hypotension, hypertension, nausea, bradycardia, atrial fibrillation, dry mouth, vomiting, hypovolemia, atelectasis, pleural effusion, agitation, tachycardia, anemia, hyperthermia, chills, hyperglycemia, and hypoxia are presented for patients receiving placebo, propofol, and dexmedetomidine. The data shows the percentage of patients experiencing these adverse reactions in each group, with hypotension and hypertension being the most common.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.