Dopamine Hydrochloride Injection
Product Images NDC 51662-1490

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 Dopamine Hydrochloride (NDC 51662-1490). 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

Dosage (Dosage)

Dosage (Dosage)
A data table showing concentration details for dopamine hydrochloride injection USP. It cross-references concentrations of 40 mg/mL and 80 mg/mL with volumes of dopamine hydrochloride injection (5 mL, 10 mL) and lists corresponding microgram per milliliter concentrations for 250 mL, 500 mL, and 1000 mL bottles of intravenous solution.*
FDA Label Image

Hs (Hs)

Hs (Hs)
A data table listing various strengths, packaging, and NDC numbers for dopamine hydrochloride injection. It details strengths ranging from 200 mg/5 mL to 800 mg/10 mL, each packaged as a carton of 25 vials, with corresponding NDC numbers provided for each.*
FDA Label Image

Serialized Label (Serialized Labeling)

Serialized Label (Serialized Labeling)
Dopamine Hydrochloride Injection, USP 400 mg/10 mL (40 mg/mL) single dose vial with a blue cap. The label includes the NDC 0143-9254-01, is marked Rx only, and shows the distributor as HF Acquisition Co., LLC. The vial size is 10 mL.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of dopamine hydrochloride, showing a benzene ring with two hydroxyl groups (OH) and an ethylamine side chain attached to hydrochloride (HCl).*
FDA Label Image

Vial (Vial Label)

Vial (Vial Label)
Label for Dopamine Hydrochloride Injection, USP, 40 mg/mL strength, in a 10 mL single dose vial. The label indicates it must be diluted and is for intravenous use. It lists inactive ingredients including sodium metabisulfite, citric acid, and sodium citrate. Manufactured by HKMA FarmacĂȘutica and distributed by West-Ward, Eatontown, NJ.*

* 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.