Dopamine Hydrochloride And Dextrose Injection, Solution
Product Images NDC 0338-1005

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Dopamine Hydrochloride And Dextrose (NDC 0338-1005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Dopamine Hydrochloride, Usp Structural Formula Image (Image 01)

Dopamine Hydrochloride, Usp Structural Formula Image (Image 01)
Chemical structure of Dopamine Hydrochloride, showing the benzene ring with two hydroxyl groups and an ethylamine side chain with associated hydrochloride.*
FDA Label Image

Dextrose Hydrous, Usp (d-gluocpyranose Monohydrate) Structural Formula Image (Image 02)

Dextrose Hydrous, Usp (d-gluocpyranose Monohydrate) Structural Formula Image (Image 02)
Chemical structure of Dopamine Hydrochloride shown as a molecular diagram including hydrogen, oxygen, and nitrogen atoms. Below it is the chemical name and formula for Dextrose Hydrous (β-Glucopyranose monohydrate). This image relates to the active ingredients in Dopamine Hydrochloride and Dextrose injection solution by Baxter Healthcare Corporation.*
FDA Label Image

Ndc 0338-1005-02 Representative Container Label (Image 03)

Ndc 0338-1005-02 Representative Container Label (Image 03)
Label for Dopamine Hydrochloride and Dextrose Injection USP, 200 mg per 250 mL (800 mcg/mL) intravenous solution. The sterile single dose container is marked with volume graduations on the side and includes detailed formulation information such as 80 mg dopamine HCl and 5 g dextrose per 100 mL, pH range, osmolarity, and storage instructions. Manufactured by Baxter Healthcare Corporation.*
FDA Label Image

Representative Carton Label 0338-1005-02 (Image 04)

Representative Carton Label 0338-1005-02 (Image 04)
Label for Dopamine Hydrochloride and 5% Dextrose injection solution, USP, with a strength of 200 mg per 250 mL. The label includes lot number T123456, NDC 0338-1005-02, expiration date JAN 9999, and a barcode. It is an intravenous solution provided by Baxter Healthcare Corporation.*
FDA Label Image

Ndc 0338-1007-02 Representative Container Label (Image 05)

Ndc 0338-1007-02 Representative Container Label (Image 05)
Label for Dopamine Hydrochloride and Dextrose Injection 400 mg per 250 mL (1,600 mcg/mL) by Baxter Healthcare Corporation. The sterile single dose container contains Dopamine Hydrochloride USP and 5% Dextrose Hydrous USP, with sodium bisulfite as stabilizer, pH 3.5 and osmolarity 269 mOsmol/L. The label includes storage and usage instructions and is marked Rx only.*
FDA Label Image

Representative Carton Label 0338-1007-02 (Image 06)

Representative Carton Label 0338-1007-02 (Image 06)
Label for Dopamine Hydrochloride and 5% Dextrose injection, USP, containing 400 mg per 250 mL. The label shows lot number, expiration date, NDC code 0338-1007-02, and barcode information. It is a solution for intravenous use.*
FDA Label Image

Ndc 0338-1009-02 Representative Container Label (Image 07)

Ndc 0338-1009-02 Representative Container Label (Image 07)
Label for Dopamine Hydrochloride and 5% Dextrose Injection USP by Baxter Healthcare Corporation. It indicates a concentration of 800 mg per 250 mL (3,200 mcg/mL) in a sterile single-dose 250 mL container. Additional text includes storage instructions, dosing guidance, and active ingredient details.*
FDA Label Image

Representative Carton Label 0338-1009-02 (Image 08)

Representative Carton Label 0338-1009-02 (Image 08)
Label for Dopamine Hydrochloride and 5% Dextrose Injection, USP, showing strength of 800 mg per 250 mL in solution form. The label includes lot number T123456, expiration date JAN 9999, and NDC 0338-1009-02. It also features barcode and QR code markings, with a quantity note of 18 bags each 250 mL. Labeled by Baxter Healthcare Corporation.*

* 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.