Dexmedetomidine Hydrochloride Injection
Product Images NDC 0338-9555

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride (NDC 0338-9555). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Company, 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 Hydrochloride In 0.9% Sodium Chloride Injection Structural Formula (Image 01)

FDA Label Image

Baxter Logo (Image 02)

This is a medication with the NDC code 0338-9555-24, which is Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection. The single dose container contains 200 mcg per 50 mL of the medication, and the usual dosage should be determined by a healthcare professional. The medication is for intravenous infusion and should be stored at 20° to 25°C. Unused portions should be discarded, and the medication should not be frozen. Bayer and Galaxy are registered trademarks of Baxter International Inc. Made in the USA.*

FDA Label Image

Dex Med Representative Container Label 0338-9555-24 (Image 03)

The text contains information about two similar products named "Galaxy Gt PL2801 Pt" and "Galaxy Gt P21 Pt". It also includes the composition and dosages of "Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection" and the related information about its usage and storage. The text also includes some codes and numbers that might be related to these products or their distribution.*

FDA Label Image

Dex Med Representative Carton Label 0338-9555-24 1 Of 2 (Image 04)

FDA Label Image

Dex Med Representative Carton Label 0338-9555-24 2 Of 2 (Image 05)

This is a description of a medication labeled as NDC0338-9557-12. The medication is Dexmedetomidine Hydrochloride, which is dissolved in 0.9% sodium chloride injection solution at a concentration of 4mg/mL. The medication is provided as 100mL IV infusion. The medication should be discarded if any unused portion is left. The medication contains 4mg Dexmedetomidine, 9mg sodium chloride, 483mg Sodium acette trihcrate, 87mg glacial acetic acid per mL in Water for Injection. The normal dosage should be as per the prescription, and the medication can be stored at 20°C-25°C temperature range. The manufacturer is Baxter and the label has a code of 263497.*

FDA Label Image

Dex Med Representative Container Label 0338-9557-12 (Image 06)

This is a description of a medical product. The product is Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection in a single dose container with a strength of 400 mg per 100 mL (4 mg/mL). It has an Rx Only label and is manufactured and distributed by Baxter Healthcare Corporation, located in Deerfield, IL. The container is made of Galaxy PL250T plastic, and the product is registered as a trademark of Baxter International Inc. The product should be stored between 20°-25°C. The codes mentioned are DG 0338-9557-12, NDC0338-9557-12, and code 263407.*

FDA Label Image

Dex Med Representative Carton Label 0338-9557-12 1 Of 2 (Image 07)

This is a description for a medication meant for IV infusion. It contains deneodetomidine, dexedetomidine, sodium chioride, sodium acefae tehydrae, and water. The usual dosage is not specified and should be determined by prescription.*

* 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.