Dexmedetomidine Hydrochloride Injection
Product Images NDC 43066-561

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride (NDC 43066-561). 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 Structural Formula (Image 01)

FDA Label Image

Dexmed Representative Container Label 43066-561-24 1 Of 2 (Image 02)

This is a medication containing Dexmedetomidine Hydrochloride, which is a sedative used for intravenous infusion. It is supplied in a 50 mL single-dose container with 200 mcg per 50 mL. Each milliliter contains 4 mgs of Dexmedetomidine Hydrochloride, 8 mgs of Sodium Chloride, 483 mgs of Sodium Acetate Trihydrate, 87 meg of Glacial Acetic Acid, and water for injection. The medication should be discarded if not used. Exact dosage information must be obtained from the prescribing information. The medication should be stored at 20° to 25°C and should not be frozen. Galaxt and PREMIERProRx are registered trademarks of Baxter International Inc. and Premier, Inc., respectively. The product is manufactured in the USA.*

FDA Label Image

Dexmed Representative Container Label 43066-561-24 2 Of 2 (Image 03)

FDA Label Image

Dexmed Representative Carton Label 43066-561-24 1 Of 2 (Image 04)

This is a product description for two different types of 0.9% Sodium Chloride Injection, both containing 200mg per 50mL of Dexmedetomidine Hydrochloride and provided in a single dose container. The first product is registered under the trademark GALAXY Container and manufactured by Baxter Healthcare Corporation in the USA, while the second product is registered under the trademark PREMIERPIORK and used under license by Premier Inc. Both products come in plastic containers and should be stored between 20°C and 25°C. The products are labeled with the National Drug Code (NDC) 43066-561-24 and should be administered under prescription only with the code 263494 being referenced. There is a bar code included, which is positioned in the same location on both products.*

FDA Label Image

Dexmed Representative Carton Label 43066-561-24 2 Of 2 (Image 05)

Each milliliter of the solution is for intravenous infusion and includes 4 milligrams of dexmedetomidine as dexmedetomidine HCL, USP, as well as other ingredients such as sodium chloride, USP and sodium acetate trihydrate, USP. The pH of the solution is 18451055. The usual dosage should be determined by prescribing information.*

FDA Label Image

Dexmed Representative Shipper Label 43066-561-24 (Image 06)

Dexmedetomidine Hydrochloride is a medication for intravenous administration. It is diluted in 0.9% Sodium Chloride Injection and contains 200 mcg per 50 mL (4 meg / mL). The medication is available with a code 2G3494 and an NDC (National Drug Code) of 43066-561-24. It should be stored at temperatures between 20°C to 25°C (68°F to 77°F). It is manufactured by Baxter Healthcare Corporation in Deerfield, IL, USA. The medication is only available on prescription.*

FDA Label Image

Dexmed Representative Container Label 43066-565-12 1 Of 2 (Image 07)

This is a medication with the National Drug Code 43066-565-12, which is administered intravenously using 0.9% Sodium Chloride Injection. It comes in a 100 mL Single Dose Container, and each mL contains 4 mcg dexmedetomidine Hydrochloride with other substances. It is stored at a controlled temperature and should not be frozen. Dosage should be determined according to the prescribing instructions. This medication is made by Baxter Healthcare Corporation, and it is a registered trademark of Premier, Inc.*

FDA Label Image

Dexmed Representative Container Label 43066-565-12 2 Of 2 (Image 08)

FDA Label Image

Dexmed Representative Carton Label 43066-565-12 1 Of 2 (Image 09)

This is a description of a container for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection. The container is manufactured by Baxter Healthcare Corporation and has the trademark names of "PremierproRx" and "Galaxy". It is made of PL2501 Plastic and contains (1x6) 100 single-dose containers with 400 mcg per 100 mL (4 mg/mL) of the solution. The container has a barcode and a code number of NDC 43066-565-12 and 263495, respectively. The solution should be stored at 20-25°C (68-71°F) and should not be frozen.*

FDA Label Image

Dexmed Representative Carton Label 43066-565-12 2 Of 2 (Image 10)

This is a medication for intravenous infusion. Each mL of the solution contains 4mg dexmedetomidine, sodium chloride, sodium acetate trihydrate, glacial acetic acid, and water for injection. The usual dosage is to be determined by the prescribing physician.*

FDA Label Image

Dexmed Representative Shipper Label 43066-565-12 (Image 11)

Dexmedetomidine Hydrochloride is a prescription drug that comes as an injection mixed with 0.9% Sodium Chloride. Each 100 mL of the solution contains 400 mcg or 4 meg per mL. The product code is 2G3495 and the NDC number is 43066-565-12. It must be stored at a temperature of 20-25°C and should not be frozen. The drug is manufactured by Baxter Healthcare Corporation located in Deerfield, IL. This drug is prescribed only by a medical professional.*

* 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.