Dexmedetomidine Hydrochloride Injection
Product Images NDC 0338-9555

7 FDA label images from Baxter Healthcare Company · Packaging, Regulatory Labels, and Product Appearance

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)

Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride Injection Structural Formula (Image 01)
Chemical structure of dexmedetomidine hydrochloride showing its molecular framework including imidazole and benzene rings, methyl groups, and hydrochloride component.*
FDA Label Image

Baxter Logo (Image 02)

Baxter Logo (Image 02)
Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg/mL) intravenous injection. The 50 mL single-dose container is labeled under the brand name GALAXY, manufactured by Baxter Healthcare Company. Storage instructions and detailed ingredient information are included on the label.*
FDA Label Image

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

Dex Med Representative Container Label 0338-9555-24 (Image 03)
Dexmedetomidine Hydrochloride 200 mcg per 50 mL injection in 0.9% Sodium Chloride, intravenous dosage form, packaged in single-dose containers of 50 mL. Label shows solution strength as 4 mcg/mL, labeled for Rx only, manufactured by Baxter Healthcare Company, USA. The label includes storage instructions and bar code placement information.*
FDA Label Image

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

Dex Med Representative Carton Label 0338-9555-24 1 Of 2 (Image 04)
A text panel providing injection instructions for dexmedetomidine hydrochloride intravenous infusion. It details the contents per mL, including dexmedetomidine hydrochloride, sodium chloride, sodium acetate trihydrate, glacial acetic acid, and water for injection, along with a pH range of 4.5 to 5.5. The panel also references usual dosage instructions found in the prescribing information.*
FDA Label Image

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

Dex Med Representative Carton Label 0338-9555-24 2 Of 2 (Image 05)
Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) intravenous injection. The single dose container of 100 mL is from Baxter Healthcare Company, featuring preparation and storage instructions including temperature range 20° to 25°C, and a note to discard unused portions.*
FDA Label Image

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

Dex Med Representative Container Label 0338-9557-12 (Image 06)
Label for Dexmedetomidine Hydrochloride 400 mcg per 100 mL (4 mcg/mL) injection in 0.9% sodium chloride. The label states Rx Only and includes storage instructions (store at 20° to 25°C, do not freeze). The product comes in single dose containers of 100 mL. The labeler is Baxter Healthcare Corporation, Deerfield, IL, USA, and the label features the Baxter logo and trademark information.*
FDA Label Image

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

Dex Med Representative Carton Label 0338-9557-12  1 Of 2 (Image 07)
Text panel detailing the formulation composition of DEXMEDETOMIDINE HYDROCHLORIDE intravenous infusion. It specifies the amount of dexmedetomidine hydrochloride and excipients per mL, including sodium chloride, sodium acetate trihydrate, glacial acetic acid, and water for injection, with pH range noted. Dosage reference directs to prescribing information.*

* 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.