Oncology & Anticancer

Daunorubicin HydrochlorideThird Party Manufacturing in India

Looking to get Daunorubicin Hydrochloride 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
23541-50-6
Drug Class
Anthracycline antineoplastic antibiotic / Topoisomerase II inhibitor
Molecular Formula
C₂₇H₂₉NO₁₀·HCl
Molecular Weight
563.98 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

Daunorubicin Hydrochloride works by binding directly to DNA to block the replication and division of leukemia cells.

The molecule intercalates between adjacent base pairs in the DNA double helix, which prevents the DNA from unwinding and halts both DNA and DNA-dependent RNA synthesis. Furthermore, it binds to and inhibits topoisomerase II, an enzyme crucial for repairing DNA tension during replication. By stabilizing the cleavage complex, it prevents DNA religation, leading to single and double-strand DNA breaks. Daunorubicin also triggers the intracellular generation of reactive oxygen species (free radicals), which damages the cell membrane and DNA structure, inducing apoptosis.

Unlike typical antimetabolites, Daunorubicin Hydrochloride is an anthracycline antibiotic that kills cells in multiple phases of the cell cycle, though it is most active during the S-phase. It is highly effective for inducing remission in pediatric and adult leukemia patients.

Therapeutic Uses & Indications

Daunorubicin Hydrochloride (CAS 23541-50-6) is a vital anthracycline chemotherapy agent widely utilized in hematological oncology. Celesta offers premier services for Daunorubicin Hydrochloride third party manufacturing in India, supplying high-quality oncology injectables to global markets.

Therapeutic Uses

Daunorubicin Hydrochloride is prescribed for the treatment of:

  • Acute Myelogenous Leukemia (AML): Used as a first-line induction chemotherapy agent in adults, often in combination with cytarabine.
  • Acute Lymphoblastic Leukemia (ALL): Indicated for remission induction in both pediatric and adult ALL cell lines.
  • Chronic Myelogenous Leukemia (CML): Used in specific chemotherapy protocols during blast crisis or when other therapies fail.

Choosing a Daunorubicin Hydrochloride Manufacturer in India

Daunorubicin Hydrochloride is listed as an essential medicine by the WHO, reflecting its critical role in leukemia therapy. Because it is a highly cytotoxic anthracycline, its production requires dedicated cytotoxic manufacturing facilities, isolated aseptic filling areas, and lyophilization equipment. Sourcing from a WHO-GMP certified manufacturer in India ensures compliance with strict environmental controls to prevent cross-contamination and protect workers. Sourcing through a WHO-GMP certified partner ensures high-quality sterile products that meet IP, BP, and USP monographs, which is essential for national health tenders and global export channels.

To place an order or discuss customization, please contact our team. You can view all our oncology injectables on our manufacturing listing or learn about our service offerings on our contract manufacturing page.

This makes Daunorubicin Hydrochloride one of the most sought-after molecules for third party manufacturing in India, with consistent demand from cancer hospitals and export-oriented distributors.

Dosage Forms We Manufacture

Injection
20mg

Frequently Asked Questions

What is the minimum order quantity for Daunorubicin Hydrochloride?
Minimum order quantity for Daunorubicin Hydrochloride is Contact us for MOQ — varies by strength and dosage form. Please contact us for bulk pricing and custom quantities.
What dosage forms of Daunorubicin Hydrochloride can you manufacture?
We manufacture Daunorubicin Hydrochloride as: Injection (20mg).
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 Daunorubicin Hydrochloride for export?
Yes. We provide export-ready Daunorubicin Hydrochloride 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 Daunorubicin Hydrochloride?
We manufacture Daunorubicin Hydrochloride to IP, BP, USP pharmacopoeial standards.
Third Party Manufacturing

Get Daunorubicin Hydrochloride 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

Single-dose USP Type I glass vials (lyophilized powder). Packaging customized to client brand guidelines.

Start Manufacturing Daunorubicin Hydrochloride Today

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

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