Oncology & Anticancer

DactinomycinThird Party Manufacturing in India

Looking to get Dactinomycin 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
50-76-0
Drug Class
Antineoplastic antibiotic / Cytotoxic transcription inhibitor
Molecular Formula
C₆₂H₈₆N₁₂O₁₆
Molecular Weight
1255.44 g/mol
Grade Standards
IP, BP, USP
Therapeutic Category
Oncology & Anticancer
MOQ
Contact us for MOQ — varies by strength and dosage form
Dosage Forms
Injection

Mechanism of Action

Dactinomycin works by binding to DNA and blocking the synthesis of RNA within rapidly dividing cancer cells.

The molecule intercalates itself into the DNA double helix, specifically binding to guanine-cytosine base pairs. This physical insertion alters the shape of the DNA template and blocks the movement of DNA-dependent RNA polymerase, thereby halting the transcription of messenger RNA. Consequently, the cell cannot produce proteins necessary for survival and division. At higher clinical concentrations, dactinomycin also inhibits DNA replication and impairs topoisomerase II, leading to DNA strand breaks and apoptosis.

Unlike synthetic chemical chemotherapy agents, Dactinomycin is a naturally derived polypeptide antibiotic that acts as a potent cell-cycle non-specific cytotoxic drug. It is highly effective for pediatric oncology patients undergoing combination treatments.

Therapeutic Uses & Indications

Dactinomycin (CAS 50-76-0) is an essential cytotoxic antibiotic used in multiple pediatric and adult cancer regimens. We offer high-quality options for Dactinomycin third party manufacturing in India, ensuring stable global access to this critical antineoplastic drug.

Therapeutic Uses

Dactinomycin is prescribed for the treatment of:

  • Wilms' Tumor: Used in combination chemotherapy regimens as standard treatment for pediatric nephroblastoma.
  • Rhabdomyosarcoma: Indicated for pediatric soft-tissue tumors, usually combined with vincristine and cyclophosphamide.
  • Gestational Trophoblastic Neoplasia: Prescribed as a first-line treatment for low-risk and high-risk gestational trophoblastic tumors.
  • Ewing's Sarcoma: Utilized in multi-agent chemotherapy regimens to treat malignant bone tumors in children and young adults.

Choosing a Dactinomycin Manufacturer in India

Dactinomycin is listed on the WHO Model List of Essential Medicines due to its irreplaceable role in pediatric oncology. Because of its high potency, manufacturing dactinomycin injection requires highly specialized aseptic processing, lyophilization technology, and dedicated cytotoxic containment areas. Sourcing from a WHO-GMP certified manufacturer in India ensures that each vial contains sterile, pyrogen-free lyophilized powder meeting the strict requirements of IP, BP, and USP standards. Partnering with a WHO-GMP certified partner allows oncology distributors to secure a steady supply for hospital tender systems and international export markets.

To start a project, please contact our team today. You can view our comprehensive range of oncology injectables in our manufacturing listing or check our contract manufacturing page for details.

This makes Dactinomycin one of the most sought-after molecules for third party manufacturing in India, with consistent demand from pediatric oncology networks and export-oriented distributors.

Dosage Forms We Manufacture

Injection
500mcg

Frequently Asked Questions

What is the minimum order quantity for Dactinomycin?
Minimum order quantity for Dactinomycin is Contact us for MOQ — varies by strength and dosage form. Please contact us for bulk pricing and custom quantities.
What dosage forms of Dactinomycin can you manufacture?
We manufacture Dactinomycin as: Injection (500mcg).
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 Dactinomycin for export?
Yes. We provide export-ready Dactinomycin 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 Dactinomycin?
We manufacture Dactinomycin to IP, BP, USP pharmacopoeial standards.
Third Party Manufacturing

Get Dactinomycin made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • Low MOQ, export ready
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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

USP Type I glass vials (lyophilized powder) with customized carton packaging. Packaging customized to client brand guidelines.

Start Manufacturing Dactinomycin Today

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

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