Cardiac & Antihypertensive

DobutamineThird Party Manufacturing in India

Looking to get Dobutamine manufactured under your brand? Our WHO-GMP certified partner facilities support PCD franchise partners and global export opportunities structured across 25+ countries.

WHO-GMP Certified
Export Ready
PCD Franchise Available
CAS Number
34368-04-2
Drug Class
Inotropic agent / Beta-1 adrenergic agonist
Molecular Formula
C₁₈H₂₃NO₃
Molecular Weight
301.38 g/mol
Grade Standards
IP, USP
Therapeutic Category
Cardiac & Antihypertensive
MOQ
5,000 vials per batch
Dosage Forms
Dry Injection

Mechanism of Action

Dobutamine works by stimulating beta-1 adrenergic receptors in the myocardium to enhance contractility. It inhibits ventricular filling pressures and systemic vascular resistance to help the body improve overall cardiac output during acute failure. Unlike non-selective sympathomimetics, it has minimal effect on heart rate and peripheral alpha receptors at therapeutic doses. Sourcing is managed via premium manufacturing lines under CAS 34368-04-2. It is highly effective and well-tolerated.

Therapeutic Uses & Indications

Therapeutic Uses

  • Cardiogenic Shock: Restores hemodynamic stability during acute cardiac pump failure or myocardial infarction.
  • Cardiac Surgery Support: Used post-operatively to treat transient myocardial stunning and maintain perfusion.
  • Dobutamine Stress Testing: Employed as a pharmacological agent during diagnostic echocardiography procedures.

Why Manufacturers Choose Dobutamine

Dobutamine is a foundational emergency cardiac drug utilized across intensive care units globally. Utilizing Dobutamine third party manufacturing in India allows pharmaceutical companies to secure scalable supplies for government tenders and institutional hospital chains. Our partner facilities offer excellent sterile validation that meets strict WHO-GMP compliance standards. This ensures high chemical stability and consistent performance under urgent clinical scenarios.

Dosage Forms We Manufacture

Dry Injection
250mg

Frequently Asked Questions

What is the minimum order quantity for Dobutamine?
Minimum order quantity for Dobutamine is 5,000 vials per batch. Please contact us for bulk pricing and custom quantities.
What dosage forms of Dobutamine can you manufacture?
We manufacture Dobutamine as: Dry Injection (250mg).
Are your manufacturing facilities WHO-GMP certified?
Yes. Celesta Healthcare works exclusively with WHO-GMP certified partner production facilities. All manufacturing batches are subject to strict quality control and documentation.
Can you manufacture Dobutamine for export?
Yes. We provide export-ready Dobutamine formulations structured across 25+ countries. We provide full export documentation including Certificate of Analysis (CoA), Certificate of Origin, and regulatory dossiers on request.
What grade standards do you follow for Dobutamine?
We manufacture Dobutamine to IP, USP pharmacopoeial standards.
Third Party Manufacturing

Get Dobutamine made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • MOQ from 5,000 vials per batch
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Our Manufacturing Capabilities

  • WHO-GMP Certified Partner Plants
  • 25+ years of pharma industry experience
  • PCD Franchise with monopoly rights
  • Export support across 25+ countries
  • Small batch to commercial scale
  • Custom formulation development

Packaging Options

Clear glass vials with tight rubber enclosures and plastic caps. Packaging customized to client brand guidelines.

Start Manufacturing Dobutamine Today

Celesta Healthcare provides WHO-GMP certified third-party manufacturing for Dobutamine across all dosage forms. PCD franchise and export orders welcome.

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