Cardiac & Antihypertensive

Enoxaparin SodiumThird Party Manufacturing in India

Looking to get Enoxaparin Sodium 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
679809-58-6
Drug Class
Low molecular weight heparin (LMWH) anticoagulant
Molecular Formula
[C₂₆H₄₀N₂O₃₆S₅]ₙ
Molecular Weight
4500 g/mol
Grade Standards
IP, BP, USP, EP
Therapeutic Category
Cardiac & Antihypertensive
MOQ
5,000 syringes per batch
Dosage Forms
Injection

Mechanism of Action

Enoxaparin Sodium works by preventing and treating blood clots by accelerating the body's natural anticoagulant mechanisms.

The molecule acts by binding to and activating antithrombin III, a naturally occurring protein that inhibits the coagulation cascade. Once bound, enoxaparin sodium dramatically accelerates the rate at which antithrombin III inactivates Factor Xa and, to a lesser extent, Factor IIa (thrombin). By neutralizing Factor Xa, the drug prevents the conversion of prothrombin to thrombin, which blocks the subsequent conversion of fibrinogen to fibrin, stopping clot formation.

Unlike unfractionated heparin, Enoxaparin Sodium has a higher ratio of Factor Xa to Factor IIa activity and binds less to plasma proteins. This key differentiator provides a more predictable anticoagulant response, longer half-life, and lower risk of heparin-induced thrombocytopenia. It is highly effective and well-tolerated for patients requiring deep vein thrombosis prophylaxis or management of acute coronary syndromes.

Therapeutic Uses & Indications

Therapeutic Uses

Enoxaparin Sodium is prescribed for the treatment of:

  • Deep Vein Thrombosis Prophylaxis: Prevents blood clots in patients undergoing abdominal, hip, or knee replacement surgeries, or in hospitalized patients with restricted mobility.
  • DVT and Pulmonary Embolism Treatment: Indicated for treating active deep vein thrombosis and pulmonary embolism, both in outpatient and inpatient settings.
  • Acute Coronary Syndromes: Managed alongside aspirin to treat unstable angina and non-ST-segment elevation myocardial infarction (NSTEMI).
  • Hemodialysis Coagulation Prevention: Used to prevent blood clot formation in the extracorporeal circulation during hemodialysis.

Why Manufacturers Choose Enoxaparin Sodium

Enoxaparin Sodium is a critical, life-saving cardiovascular drug with enormous global demand. Because it is the gold standard low molecular weight heparin (LMWH), hospitals, cardiac clinics, and emergency departments procure it in massive, continuous volumes. For third party manufacturers, producing enoxaparin requires sophisticated sterile fill-finish capabilities, typically in pre-filled syringes (PFS) with integrated safety devices. Sourcing from a WHO-GMP certified facility in India ensures complex biopolymer stability, strict endotoxin controls, and high-quality standards suitable for regulated domestic and export markets.

This makes Enoxaparin Sodium one of the most sought-after anticoagulants for third party manufacturing in India, with consistent demand from PCD franchise operators and export-oriented companies.

Dosage Forms We Manufacture

Injection
Contact us for strengths

Frequently Asked Questions

What is the minimum order quantity for Enoxaparin Sodium?
Minimum order quantity for Enoxaparin Sodium is 5,000 syringes per batch. Please contact us for bulk pricing and custom quantities.
What dosage forms of Enoxaparin Sodium can you manufacture?
We manufacture Enoxaparin Sodium as: Injection (Contact us for strengths).
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 Enoxaparin Sodium for export?
Yes. We provide export-ready Enoxaparin Sodium 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 Enoxaparin Sodium?
We manufacture Enoxaparin Sodium to IP, BP, USP, EP pharmacopoeial standards.
Third Party Manufacturing

Get Enoxaparin Sodium made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • MOQ from 5,000 syringes 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

Pre-filled syringes (PFS) with safety needle shield device, packed in blister trays inside a printed carton.

Start Manufacturing Enoxaparin Sodium Today

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

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