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Dopamine

Generic Name
Dopamine
Brand Names
Neoatricon
Drug Type
Small Molecule
Chemical Formula
C8H11NO2
CAS Number
51-61-6
Unique Ingredient Identifier
VTD58H1Z2X

Overview

One of the catecholamine neurotransmitters in the brain. It is derived from tyrosine and is the precursor to norepinephrine and epinephrine. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (receptors, dopamine) mediate its action.

Indication

For the correction of hemodynamic imbalances present in the shock syndrome due to myocardial infarction, trauma, endotoxic septicemia, open-heart surgery, renal failure, and chronic cardiac decompensation as in congestive failure

Associated Conditions

  • Arrhythmia
  • Circulatory collapse and shock
  • Hypotension caused by Trauma, endotoxic septicemia, Open-heart Surgery, Renal Failure, chronic cardiac decompensation, Myocardial Infarction
  • Urine flow decreased caused by Trauma, endotoxic septicemia, Open-heart Surgery, Renal Failure, chronic cardiac decompensation, Myocardial Infarction
  • Decreased cardiac output caused by Trauma, endotoxic septicemia, Open-heart Surgery, Renal Failure, chronic cardiac decompensation, Myocardial Infarction

Research Report

Published: Aug 25, 2025

A Comprehensive Monograph on Dopamine (DB00988): Pharmacology, Clinical Utility, and Safety Profile

Executive Summary

Dopamine, an endogenous catecholamine, holds a dual identity of profound significance in medicine: it is both an essential neurotransmitter that governs fundamental brain functions and a potent, intravenously administered sympathomimetic agent indispensable in critical care. As a neurotransmitter, its discovery and the elucidation of its role in motor control and reward pathways revolutionized neuroscience and led to breakthrough treatments for conditions like Parkinson's disease. As a pharmaceutical agent, identified by DrugBank ID DB00988 and CAS Number 51-61-6, it is a cornerstone therapy for the management of severe hemodynamic instability.

The pharmacological profile of intravenous dopamine is distinguished by a unique dose-dependent mechanism of action. At low infusion rates, it primarily stimulates dopaminergic receptors, promoting renal and mesenteric vasodilation. At intermediate rates, it exerts positive inotropic and chronotropic effects through beta-1 adrenergic receptor stimulation, enhancing cardiac output. At high rates, it acts on alpha-1 adrenergic receptors, causing systemic vasoconstriction to increase blood pressure. This therapeutic versatility allows clinicians to titrate the drug to achieve specific physiological goals in the management of shock syndromes arising from diverse etiologies such as myocardial infarction, septicemia, and major surgery.

Continue reading the full research report

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/08/08
Not Applicable
Not yet recruiting
2024/09/25
Phase 1
Recruiting
2024/06/21
Not Applicable
Completed
2024/06/07
Not Applicable
Recruiting
2023/02/16
Not Applicable
Recruiting
2022/04/26
N/A
Recruiting
2021/02/12
Not Applicable
UNKNOWN
Szeged University
2020/09/02
Phase 3
Completed
2020/08/25
Phase 2
UNKNOWN
2019/09/27
Phase 4
Recruiting
Leiden University Medical Center

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Hospira, Inc.
0409-5820
INTRAVENOUS
40 mg in 1 mL
9/21/2023
Dr. Donna Restivo DC
62185-0050
ORAL
6 [hp_X] in 1 mL
5/23/2025
HF Acquisition Co LLC, DBA HealthFirst
51662-1291
INTRAVENOUS
40 mg in 1 mL
2/22/2024
HF Acquisition Co LLC, DBA HealthFirst
51662-1458
INTRAVENOUS
1.6 mg in 1 mL
1/27/2024
Medical Purchasing Solutions, LLC
71872-7066
INTRAVENOUS
40 mg in 1 mL
5/30/2023
Dr. Donna Restivo DC
62185-0059
ORAL
8 [hp_X] in 1 mL
5/23/2025
Henry Schein, Inc.
0404-9981
INTRAVENOUS
40 mg in 1 mL
2/17/2022
Hikma Pharmaceuticals USA Inc.
0143-9254
INTRAVENOUS
40 mg in 1 mL
5/6/2022
Baxter Healthcare Corporation
0338-1005
INTRAVENOUS
80 mg in 100 mL
7/14/2017
ProPharma Distribution
84549-252
INTRAVENOUS
40 mg in 1 mL
6/23/2025

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
TROPIN 200 INJECTION 200 mg/5 ml
SIN11216P
INJECTION
200 mg/5 ml
11/4/1999

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

TGA Drug Approvals

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
DOPAMINE HCL 1.6MG/ML DEXTROSE 5% INJ USP
baxter corporation
00761826
Solution - Intravenous
1.6 MG / ML
12/31/1990
DOPAMINE HCL 0.8MG/ML DEXTROSE 5% INJ USP
baxter corporation
00761850
Solution - Intravenous
0.8 MG / ML
12/31/1992
DOPAMINE HYDROCHLORIDE AND 5% DEXTROSE INJECTION USP
hospira healthcare ulc
00619701
Solution - Intravenous
0.8 MG / ML
12/31/1986
DOPAMINE HYDROCHLORIDE AND 5% DEXTROSE INJECTION USP
hospira healthcare ulc
00619698
Solution - Intravenous
1.6 MG / ML
12/31/1986
DOPAMINE HCL 3.2MG/ML DEXTROSE 5% INJ USP
baxter corporation
00761834
Solution - Intravenous
3.2 MG / ML
12/31/1990
DOPAMINE HYDROCHLORIDE AND 5% DEXTROSE INJECTION USP
hospira healthcare ulc
00782394
Solution - Intravenous
3.2 MG / ML
12/31/1991
INTROPIN INJECTION 40MG/ML
bristol-myers squibb canada
01914014
Solution - Intravenous
40 MG / ML
12/31/1993
DOPAMINE HCL INJ 4%
International Medication Systems Ltd.
00423823
Liquid - Intravenous
40 MG / ML
12/31/1980

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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