Dobutamine In Dextrose Injection, Solution
Product Images NDC 51662-1697

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dobutamine In Dextrose (NDC 51662-1697). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Label (51662 1697 1 Rfid)

Label (51662 1697 1 Rfid)
Data matrix barcode label for Dobutamine in Dextrose injection solution, distributed by HF Acquisition Co LLC in Mukilteo, WA. The label includes GTIN, expiration date, lot number, and a note to see manufacturer's insert. Marked for prescription use only (RX ONLY).*
FDA Label Image

Structure (51662 1697 1 Structure 2)

Structure (51662 1697 1 Structure 2)
Chemical structure of dobutamine in dextrose showing the molecular arrangement of the active ingredient alongside a water molecule (H2O). The diagram highlights key functional groups and ring formations relevant to the compound.*
FDA Label Image

Structure (51662 1697 1 Structure)

Structure (51662 1697 1 Structure)
Chemical structure diagram of Dobutamine hydrochloride, showing its molecular formula C18H23NO3·HCl and molecular weight of 337.85.*
FDA Label Image

Table (51662 1697 1 Table 1)

Table (51662 1697 1 Table 1)
A text panel showing example calculations for infusion rates of Dobutamine in Dextrose Injection, Solution. It includes formulas and examples calculating infusion rates in mL/h based on dose in mcg/kg/min, patient weight in kg, and solution concentration in mcg/mL.*
FDA Label Image

Label (51662 1697 1 Source Drug Label)

Label (51662 1697 1 Source Drug Label)
Label for DOBUTamine in 5% Dextrose Injection, USP, 250 mg/250 mL (1,000 mcg/mL) single-dose intravenous injection. The 250 mL container label includes lot and expiration placeholders, barcode, and red text detailing composition, warnings, storage instructions, and manufacturer/distributor information identifying Hospira, Inc. and stating it is made in Italy.*

* 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.