Precedex Injection, Solution
Product Images NDC 0409-0155

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Precedex (NDC 0409-0155). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Chemical Structure (Precedex 01)

FDA Label Image

Principal Display Panel (50 mL Bottle Label)

Principal Display Panel (50 mL Bottle Label)
LIFT is a medication containing 4 mg/dexmedetomidine and 9 mg of sodium chloride in water for intravenous use. It is stored between 20°C to 25°C and is not made of natural rubber latex. The dosage must be determined by prescription information. The text contains a product code and a barcode.*
FDA Label Image

Principal Display Panel (50 mL Bottle Tray)

FDA Label Image

Principal Display Panel (100 mL Bottle Label)

Principal Display Panel (100 mL Bottle Label)
This is a product information sheet for a prescription medication called Dexmedetomidine HCl. The sheet includes information about recommended dosage, storage instructions, and the fact that the medication is preservative-free and free of natural rubber latex; the sheet also lists the medication as being sold by Hospira, Inc. Additionally, the sheet contains information on the national drug code for the medication and a trademark disclaimer.*
FDA Label Image

Principal Display Panel (100 mL Bottle Tray)

Principal Display Panel (100 mL Bottle Tray)
This is an output of a label for an injectable medicine. The medicine is Dexmedetomidine HCl, and the brand name is Precedex. The injection comes in a 100ml single-use bottle, containing 400 mcg/100mL. The National Drug Code is NDC0409-015502. The label warns that unused portions should be discarded, and the medicine is only for RxOnly use. The rest of the text appears to be difficult to read accurately, containing many errors and missing information.*
FDA Label Image

Premierprorx Logo (Precedex2)

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