Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride Injection
Product Images NDC 43066-557

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Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride (NDC 43066-557). 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 43066-555-24 1 Of 2 (Image 02)

Dexmed Representative Container Label 43066-555-24 1 Of 2 (Image 02)
This is a medication with the NDC code 43066-555-24 consisting of Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection with a concentration of 200 mcg per 50 mL. It comes in a single dose container bearing the Galaxy Code 263452 and is intended for Intravenous Infusion only. Each mL of this medication contains 4 mcg dexmedatomidine provided as 472 mcg domedetomidine HC, USP along with sodium chloride, sodium acetate trihydrate, glacial acetic acid, and Waar for hiecton, USP. This drug must be stored between 5 and 25 degrees Celsius, and it is not recommended to freeze it. It is manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015 USA. The usual dosage is not available.*
FDA Label Image

Dexmed Representative Container Label 43066-555-24 2 Of 2 (Image 03)

FDA Label Image

Dex Med Representative Carton Label 43066-555-24 1 Of 3 (Image 04)

Dex Med Representative Carton Label 43066-555-24 1 Of 3 (Image 04)
The text describes a plastic container with the trademark name "GALAXY Container PL2501". It is manufactured in the USA by Baxter Healthcare Corporation and has the trademark "Novaplus". The container is also marked with a serial number "0078488".*
FDA Label Image

Dex Med Representative Carton Label 43066-555-24 2 Of 3 (Image 05)

Dex Med Representative Carton Label 43066-555-24 2 Of 3 (Image 05)
This is a description of Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, which comes in 200 microgram per 50 mL concentration. The product is packaged in 12 single-dose containers of 50 mL each, and should be stored at room temperature between 20°C and 25°C. The product is intended for use by prescription only, and has an NDC code of 43066-565-24 and a Code of 2G3492, which are provided as barcodes on the packaging.*
FDA Label Image

Dex Med Representative Carton Label 43066-555-24 3 Of 3 (Image 06)

Dex Med Representative Carton Label 43066-555-24 3 Of 3 (Image 06)
The text describes the ingredients present in an intravenous infusion medication, including dexmedetomidine, sodium chloride, sodium acetate trihydrate, glacial acetic acid, and water for injection. The pH level is noted as 4.5 to 5.5, and the usual dosage information is available in the prescribing information.*
FDA Label Image

Dexmed Representative Container Label 43066-557-24 1 Of 2 (Image 07)

Dexmed Representative Container Label 43066-557-24 1 Of 2 (Image 07)
This is a medication with the NDC code 33065-557-12 called Dexmedetom. It is a solution for intravenous infusion, each 100ml containing 400mcg of dexmedetomidine hydrochloride, USP, and other ingredients. The usual dosage should be provided by a physician and unused portions should be discarded. This medication is registered under the trademark Novaplus. It is manufactured by Baxter Healthcare Corporation in the US and should be stored between 20° to 25°C.*
FDA Label Image

Dexmed Representative Container Label 43066-557-24 2 Of 2 (Image 08)

FDA Label Image

Dex Med Representative Carton Label 43066-557-12 1 Of 3 (Image 09)

Dex Med Representative Carton Label 43066-557-12 1 Of 3 (Image 09)
This is a description of a plastic container with the brand name "GALAXY" and model "PL2501". It is made in the USA by Baxter Healthcare Corporation in Deerfield. The product is associated with the registered trademarks "Galaxy" and "Novaplus". The text appears to contain an identification number for "novaplus" but it is challenging to read due to errors.*
FDA Label Image

Dex Med Representative Carton Label 43066-557-12 2 Of 3 (Image 10)

Dex Med Representative Carton Label 43066-557-12 2 Of 3 (Image 10)
This is a description of Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection. Each container has 400mcg per 100mL of Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection. It comes in a pack of 6 single-dose containers which should be stored between 20°C to 25°C. The product shouldn't be frozen. The product has an NDC code of 43066-557-12 and a code of 2G3493. The barcode position is only for the NDC and code.*
FDA Label Image

Dex Med Representative Carton Label 43066-557-12 3 Of 3 (Image 11)

Dex Med Representative Carton Label 43066-557-12 3 Of 3 (Image 11)
This is a description of an Intravenous Infusion medication which contains 4 mog dexmedetomidine, sodium chloride, sodium acetate trihydrate, glacial acetic acid, and water for injection. The pH level is between 4.5 and 5.5. The dosage information is not provided and referring to its prescribing information is necessary.*

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