Respiratory & Allergy

DesloratadineThird Party Manufacturing in India

Looking to get Desloratadine 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
100643-71-8
Drug Class
Third-generation antihistamine (piperidine)
Molecular Formula
C₁₉H₁₉ClN₂
Molecular Weight
310.82 g/mol
Grade Standards
IP, USP, BP
Therapeutic Category
Respiratory & Allergy
MOQ
1,000 tablets per batch
Dosage Forms
Tablet

Mechanism of Action

Desloratadine is a long-acting tricyclic histamine antagonist with selective and peripheral H1-receptor antagonist activity. It is the active descarboethoxy metabolite of loratadine and represents a third-generation antihistamine. Histamine is a chemical mediator released from mast cells and basophils during allergic reactions that binds to H1 receptors on target cells, triggering symptoms such as nasal congestion, sneezing, watery eyes, and itching. Desloratadine competes with free histamine for binding at H1-receptors in the gastrointestinal tract, uterus, large blood vessels, and bronchial smooth muscle. This competitive blockade prevents histamine-mediated cellular activation and the subsequent release of additional inflammatory mediators. Unlike first-generation antihistamines, desloratadine does not readily cross the blood-brain barrier because of its molecular structure and physicochemical properties, which means it produces significantly less sedation and cognitive impairment. At a concentration of 2 to 3 ng/mL, desloratadine shows significant interaction with the human histamine H1-receptor. The drug also inhibits histamine release from human mast cells in vitro, suggesting additional mast cell stabilizing properties beyond simple receptor blockade.

Therapeutic Uses & Indications

Therapeutic Uses

Desloratadine is prescribed for the symptomatic relief of:

  • Seasonal Allergic Rhinitis: Desloratadine effectively relieves symptoms including sneezing, rhinorrhea, nasal congestion, and itchy nose and throat associated with seasonal allergies.
  • Perennial Allergic Rhinitis: The drug provides year-round relief from chronic allergic rhinitis symptoms caused by indoor allergens such as dust mites, pet dander, and mold.
  • Chronic Idiopathic Urticaria: Desloratadine reduces the frequency and severity of hives and associated itching in patients with chronic urticaria of unknown cause.
  • Allergic Dermatitis and Conjunctivitis: It is also used off-label for other allergic conditions involving the skin and eyes.

Why Manufacturers Choose Desloratadine

Desloratadine is one of the most widely prescribed antihistamines globally due to its non-sedating profile, once-daily dosing convenience, and excellent safety record. The Indian pharmaceutical industry manufactures desloratadine at scale, catering to both domestic PCD franchise networks and export markets across Asia, Africa, and the Middle East. The molecule offers manufacturers a stable regulatory pathway with established monographs in IP, USP, and BP pharmacopoeias. Its consistent demand, combined with relatively straightforward formulation chemistry, makes desloratadine a preferred molecule for third party manufacturing in India. The tablet dosage form at 5mg strength accounts for the majority of production volume, with manufacturers focusing on WHO-GMP compliant facilities to serve both branded and generic markets.

Dosage Forms We Manufacture

Tablet
5mg

Frequently Asked Questions

What is the minimum order quantity for Desloratadine?
Minimum order quantity for Desloratadine is 1,000 tablets per batch. Please contact us for bulk pricing and custom quantities.
What dosage forms of Desloratadine can you manufacture?
We manufacture Desloratadine as: Tablet (5mg).
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 Desloratadine for export?
Yes. We provide export-ready Desloratadine 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 Desloratadine?
We manufacture Desloratadine to IP, USP, BP pharmacopoeial standards.
Third Party Manufacturing

Get Desloratadine made under your brand

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

Blister pack (Alu-Alu), Strip pack, HDPE bottle. Packaging customized to client brand guidelines.

Start Manufacturing Desloratadine Today

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

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