Oncology & Anticancer

CyclophosphamideThird Party Manufacturing in India

Looking to get Cyclophosphamide 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
50-18-0
Drug Class
Alkylating agent (Nitrogen mustard)
Molecular Formula
C₇H₁₅Cl₂N₂O₂P
Molecular Weight
261.09 g/mol
Grade Standards
IP, BP, USP, EP
Therapeutic Category
Oncology & Anticancer
MOQ
1,000 vials per batch
Dosage Forms
Injection

Mechanism of Action

Cyclophosphamide works by interfering with the growth and replication of cancer cells by damaging their DNA structure.

As a prodrug, Cyclophosphamide is inactive until it undergoes metabolic activation in the liver by cytochrome P450 enzymes to form active metabolites, including phosphoramide mustard and acrolein. Phosphoramide mustard acts as an alkylating agent, binding to DNA and creating cross-links between guanine bases in the double helix. These covalent interstrand and intrastrand cross-links prevent the DNA strands from separating and uncoiling, which directly blocks DNA replication and RNA transcription. This disruption triggers programmed cell death (apoptosis) in rapidly dividing cells.

Unlike cell-cycle-specific agents, Cyclophosphamide is cell-cycle nonspecific, meaning it exerts its cytotoxic effects throughout all phases of cell division. It is widely recognized for both its powerful antineoplastic properties and its immunosuppressive effects, making it a cornerstone therapy in multi-agent oncology protocols and autoimmune disease management.

Therapeutic Uses & Indications

Therapeutic Uses

Cyclophosphamide is prescribed for the treatment of:

  • Malignant Lymphomas: Used as a primary component in chemotherapy regimens for Hodgkin's disease, lymphocytic lymphoma, and histiocytic lymphoma.
  • Leukemias: Indicated for the treatment of chronic lymphocytic leukemia (CLL), chronic myelogenous leukemia (CML), and acute leukemias.
  • Breast Cancer: Utilized in combination regimens for adjuvant therapy or metastatic disease.
  • Immunosuppression: Prescribed for severe autoimmune conditions such as lupus nephritis, ANCA-associated vasculitis, and minimal change nephrotic syndrome in pediatric patients.

Why Manufacturers Choose Cyclophosphamide

Cyclophosphamide is a widely used antineoplastic agent with constant global demand, listed on the WHO Model List of Essential Medicines. Because it is a foundational drug in both oncology and rheumatology, it is purchased in large quantities by hospitals, research clinics, and international distribution agencies.

For third party manufacturers, producing Cyclophosphamide requires specialized, high-containment sterile facility lines. As a cytotoxic nitrogen mustard derivative, its handling demands advanced engineering controls, isolator technology, and dedicated production blocks to prevent cross-contamination. Sourcing from a WHO-GMP certified manufacturer in India provides distributors with compliance assurance, high-quality standards, and reliable supply continuity for critical oncology care portfolios.

This makes Cyclophosphamide one of the most sought-after molecules for third party manufacturing in India, with consistent demand from oncology hospitals and export-oriented companies.

Dosage Forms We Manufacture

Injection
200mg · 500mg · 1000mg

Frequently Asked Questions

What is the minimum order quantity for Cyclophosphamide?
Minimum order quantity for Cyclophosphamide is 1,000 vials per batch. Please contact us for bulk pricing and custom quantities.
What dosage forms of Cyclophosphamide can you manufacture?
We manufacture Cyclophosphamide as: Injection (200mg, 500mg, 1000mg).
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 Cyclophosphamide for export?
Yes. We provide export-ready Cyclophosphamide 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 Cyclophosphamide?
We manufacture Cyclophosphamide to IP, BP, USP, EP pharmacopoeial standards.
Third Party Manufacturing

Get Cyclophosphamide made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • MOQ from 1,000 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

Sterile glass vial, packed in a protective carton. Customized bulk and export-ready packaging options available.

Start Manufacturing Cyclophosphamide Today

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

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